Are you over 18 and want to see adult content?
More Annotations
A complete backup of star.ettoday.net/news/1633507
Are you over 18 and want to see adult content?
A complete backup of stars.udn.com/star/story/10087/4308856
Are you over 18 and want to see adult content?
A complete backup of www.hurriyet.com.tr/kelebek/televizyon/bir-zamanlar-cukurovanin-yeni-bolum-fragmani-yayinlandi-mi-bir-zaman
Are you over 18 and want to see adult content?
A complete backup of pomorska.pl/skoki-zakopane-2020-kiedy-konkurs-o-ktorej-skoki-ps-zakopane-program-godziny-transmisja-tv-onli
Are you over 18 and want to see adult content?
Favourite Annotations
A complete backup of https://ruebourbon.com
Are you over 18 and want to see adult content?
A complete backup of https://marshcommercial.co.uk
Are you over 18 and want to see adult content?
A complete backup of https://allianceonline.co.uk
Are you over 18 and want to see adult content?
A complete backup of https://tltpravda.ru
Are you over 18 and want to see adult content?
A complete backup of https://uneed.ir
Are you over 18 and want to see adult content?
A complete backup of https://luenen.de
Are you over 18 and want to see adult content?
A complete backup of https://peuteren.nl
Are you over 18 and want to see adult content?
A complete backup of https://weighttogo.online
Are you over 18 and want to see adult content?
A complete backup of https://kooth.com
Are you over 18 and want to see adult content?
A complete backup of https://thea.codes
Are you over 18 and want to see adult content?
A complete backup of https://gregkucera.com
Are you over 18 and want to see adult content?
A complete backup of https://listingprowp.com
Are you over 18 and want to see adult content?
Text
session.
TEMPERATURE AND HUMIDITY VALIDATION/MAPPING IN STORAGE Temperature and humidity are important factors in the stability of the pharmaceutical ingredients. Temperature sensitive materials can degrade at a higher temperature, therefore, it important to validate the storage area for temperature. PHARMACEUTICAL GUIDELINES : TOTAL PHARMACEUTICAL SOLUTIONSOPSQUALITY CONTROLQUALITY ASSURANCEMICROBIOLOGYPRODUCTIONVALIDATION If you are preparing for any regulatory inspection then gap analysis can help in compliance with regulatory guidelines. A comparison between the regulatory guidance and current practices is SOPS FOR MICROBIOLOGY : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for microbiology department (sterile and non-sterile) in pharmaceutical products manufacturing facility. FAULT TREE ANALYSIS FOR INVESTIGATION : PHARMACEUTICAL Fault Tree Analysis for Investigation You will find many articles on fault tree analysis but this is actual method with example by which you can actually prepare a fault tree diagram for the events or problems you found in pharmaceutical manufacturing industry. SOP FOR ACCEPTABLE QUALITY LEVEL (AQL) : PHARMACEUTICAL 5.5.1 If the no. of major /minor reject is at higher side. 5.5.2 If the results of AQL does not comply with the accept level. 5.6 If the cumulative total of a different defective sample in critical / major / minor category exceeds the stated ‘accept’ level, follow instruction 5.5 and again carry out AQL test as per procedure. SOP FOR PROCESS VALIDATION : PHARMACEUTICAL GUIDELINES 1.0 OBJECTIVE The purpose of this SOP is to lay down the minimum requirements for validation or revalidation of manufacturing processes applicable to marketed drug products in order to provide documented evidence that each specific process will consistently yield a product meeting all quality and design specifications. SOP FOR GOOD LABORATORY PRACTICE (GLP) : PHARMACEUTICAL Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask ROLE OF REGULATORY AFFAIRS IN PHARMACEUTICALS Regulatory affairs in pharmaceuticals are like vehicle inspectors in the automotive industry. They assess and perform quality checks to ensure that the medicinal drugs, veterinary drugs, and nutritional supplements rolled out by the pharmaceutical industry are safe and effective for the consumers to use. OCCUPATIONAL EXPOSURE BANDS (OEBS) FOR CHEMICALS Occupational exposure bands are measures put in place to categorize chemicals so that the health of the worker is not compromised. This is because Active Pharmaceutical Ingredients can have serious and adverse effects on the worker when they become lowly airborne. QUALIFICATION PROCEDURE FOR VIAL WASHING MACHINE Procedure: About 3000 vials of the selected size are loaded on the feed belt and vial washing machine is operated as per the standard operating procedure. Place the spiked vials marked with permanent marker in between the other vials while the machine is running. These vials should be placed at the initial, middle and end of the washingsession.
TEMPERATURE AND HUMIDITY VALIDATION/MAPPING IN STORAGE Temperature and humidity are important factors in the stability of the pharmaceutical ingredients. Temperature sensitive materials can degrade at a higher temperature, therefore, it important to validate the storage area for temperature. SOPS FOR MICROBIOLOGY : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for microbiology department (sterile and non-sterile) in pharmaceutical products manufacturing facility. SOP FOR GOOD LABORATORY PRACTICE (GLP) : PHARMACEUTICAL Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask SOPS FOR QUALITY CONTROL : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for Quality Control laboratories in pharmaceutical products manufacturing facilities. SOP FOR FIRST AID : PHARMACEUTICAL GUIDELINES 1.0 OBJECTIVE To lay down the procedure to render immediate first aid in an emergency to preserve life and assist recovery. 2.0 SCOPE This procedure is applicable for a casualty for any injury or sudden illness before the arrival of a qualified medical expert. ROLE OF REGULATORY AFFAIRS IN PHARMACEUTICALS Regulatory affairs in pharmaceuticals are like vehicle inspectors in the automotive industry. They assess and perform quality checks to ensure that the medicinal drugs, veterinary drugs, and nutritional supplements rolled out by the pharmaceutical industry are safe and effective for the consumers to use. SOP FOR STARTING AND STOPPING OF BOILERS : PHARMACEUTICAL Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask CAUSES AND REMEDIES OF LAMINATION IN TABLET MANUFACTURING An ideal tablet should be free from any visual defects as well as the functional defects. Despite the advancements and innovations in the manufacturing of tablets, the problems that are often encountered in the production have not decreased but instead increased. SOP FOR SAMPLING AND TESTING OF PURE STEAM 1.0 PURPOSE To lay down the procedure for the sampling of Pure steam for Microbiological and Chemical analysis. 2.0 SCOPE It is applicable to Microbiology Laboratory SOP FOR OPERATION AND MAINTENANCE OF FOGGER Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask METHOD OF ANALYSIS FOR SODIUM HYDROXIDE : PHARMACEUTICAL Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask PHARMACEUTICAL GUIDELINES : TOTAL PHARMACEUTICAL SOLUTIONSOPSQUALITY CONTROLQUALITY ASSURANCEMICROBIOLOGYPRODUCTIONVALIDATION If you are preparing for any regulatory inspection then gap analysis can help in compliance with regulatory guidelines. A comparison between the regulatory guidance and current practices is SOPS FOR MICROBIOLOGY : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for microbiology department (sterile and non-sterile) in pharmaceutical products manufacturing facility. FAULT TREE ANALYSIS FOR INVESTIGATION : PHARMACEUTICAL Fault Tree Analysis for Investigation You will find many articles on fault tree analysis but this is actual method with example by which you can actually prepare a fault tree diagram for the events or problems you found in pharmaceutical manufacturing industry. SOP FOR ACCEPTABLE QUALITY LEVEL (AQL) : PHARMACEUTICAL 5.5.1 If the no. of major /minor reject is at higher side. 5.5.2 If the results of AQL does not comply with the accept level. 5.6 If the cumulative total of a different defective sample in critical / major / minor category exceeds the stated ‘accept’ level, follow instruction 5.5 and again carry out AQL test as per procedure. SOP FOR PROCESS VALIDATION : PHARMACEUTICAL GUIDELINES 1.0 OBJECTIVE The purpose of this SOP is to lay down the minimum requirements for validation or revalidation of manufacturing processes applicable to marketed drug products in order to provide documented evidence that each specific process will consistently yield a product meeting all quality and design specifications. SOP FOR GOOD LABORATORY PRACTICE (GLP) : PHARMACEUTICAL Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask ROLE OF REGULATORY AFFAIRS IN PHARMACEUTICALS Regulatory affairs in pharmaceuticals are like vehicle inspectors in the automotive industry. They assess and perform quality checks to ensure that the medicinal drugs, veterinary drugs, and nutritional supplements rolled out by the pharmaceutical industry are safe and effective for the consumers to use. OCCUPATIONAL EXPOSURE BANDS (OEBS) FOR CHEMICALS Occupational exposure bands are measures put in place to categorize chemicals so that the health of the worker is not compromised. This is because Active Pharmaceutical Ingredients can have serious and adverse effects on the worker when they become lowly airborne. QUALIFICATION PROCEDURE FOR VIAL WASHING MACHINE Procedure: About 3000 vials of the selected size are loaded on the feed belt and vial washing machine is operated as per the standard operating procedure. Place the spiked vials marked with permanent marker in between the other vials while the machine is running. These vials should be placed at the initial, middle and end of the washingsession.
TEMPERATURE AND HUMIDITY VALIDATION/MAPPING IN STORAGE Temperature and humidity are important factors in the stability of the pharmaceutical ingredients. Temperature sensitive materials can degrade at a higher temperature, therefore, it important to validate the storage area for temperature. PHARMACEUTICAL GUIDELINES : TOTAL PHARMACEUTICAL SOLUTIONSOPSQUALITY CONTROLQUALITY ASSURANCEMICROBIOLOGYPRODUCTIONVALIDATION If you are preparing for any regulatory inspection then gap analysis can help in compliance with regulatory guidelines. A comparison between the regulatory guidance and current practices is SOPS FOR MICROBIOLOGY : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for microbiology department (sterile and non-sterile) in pharmaceutical products manufacturing facility. FAULT TREE ANALYSIS FOR INVESTIGATION : PHARMACEUTICAL Fault Tree Analysis for Investigation You will find many articles on fault tree analysis but this is actual method with example by which you can actually prepare a fault tree diagram for the events or problems you found in pharmaceutical manufacturing industry. SOP FOR ACCEPTABLE QUALITY LEVEL (AQL) : PHARMACEUTICAL 5.5.1 If the no. of major /minor reject is at higher side. 5.5.2 If the results of AQL does not comply with the accept level. 5.6 If the cumulative total of a different defective sample in critical / major / minor category exceeds the stated ‘accept’ level, follow instruction 5.5 and again carry out AQL test as per procedure. SOP FOR PROCESS VALIDATION : PHARMACEUTICAL GUIDELINES 1.0 OBJECTIVE The purpose of this SOP is to lay down the minimum requirements for validation or revalidation of manufacturing processes applicable to marketed drug products in order to provide documented evidence that each specific process will consistently yield a product meeting all quality and design specifications. SOP FOR GOOD LABORATORY PRACTICE (GLP) : PHARMACEUTICAL Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask ROLE OF REGULATORY AFFAIRS IN PHARMACEUTICALS Regulatory affairs in pharmaceuticals are like vehicle inspectors in the automotive industry. They assess and perform quality checks to ensure that the medicinal drugs, veterinary drugs, and nutritional supplements rolled out by the pharmaceutical industry are safe and effective for the consumers to use. OCCUPATIONAL EXPOSURE BANDS (OEBS) FOR CHEMICALS Occupational exposure bands are measures put in place to categorize chemicals so that the health of the worker is not compromised. This is because Active Pharmaceutical Ingredients can have serious and adverse effects on the worker when they become lowly airborne. QUALIFICATION PROCEDURE FOR VIAL WASHING MACHINE Procedure: About 3000 vials of the selected size are loaded on the feed belt and vial washing machine is operated as per the standard operating procedure. Place the spiked vials marked with permanent marker in between the other vials while the machine is running. These vials should be placed at the initial, middle and end of the washingsession.
TEMPERATURE AND HUMIDITY VALIDATION/MAPPING IN STORAGE Temperature and humidity are important factors in the stability of the pharmaceutical ingredients. Temperature sensitive materials can degrade at a higher temperature, therefore, it important to validate the storage area for temperature. SOPS FOR MICROBIOLOGY : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for microbiology department (sterile and non-sterile) in pharmaceutical products manufacturing facility. SOP FOR GOOD LABORATORY PRACTICE (GLP) : PHARMACEUTICAL Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask SOPS FOR QUALITY CONTROL : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for Quality Control laboratories in pharmaceutical products manufacturing facilities. SOP FOR FIRST AID : PHARMACEUTICAL GUIDELINES 1.0 OBJECTIVE To lay down the procedure to render immediate first aid in an emergency to preserve life and assist recovery. 2.0 SCOPE This procedure is applicable for a casualty for any injury or sudden illness before the arrival of a qualified medical expert. ROLE OF REGULATORY AFFAIRS IN PHARMACEUTICALS Regulatory affairs in pharmaceuticals are like vehicle inspectors in the automotive industry. They assess and perform quality checks to ensure that the medicinal drugs, veterinary drugs, and nutritional supplements rolled out by the pharmaceutical industry are safe and effective for the consumers to use. SOP FOR STARTING AND STOPPING OF BOILERS : PHARMACEUTICAL Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask CAUSES AND REMEDIES OF LAMINATION IN TABLET MANUFACTURING An ideal tablet should be free from any visual defects as well as the functional defects. Despite the advancements and innovations in the manufacturing of tablets, the problems that are often encountered in the production have not decreased but instead increased. SOP FOR SAMPLING AND TESTING OF PURE STEAM 1.0 PURPOSE To lay down the procedure for the sampling of Pure steam for Microbiological and Chemical analysis. 2.0 SCOPE It is applicable to Microbiology Laboratory SOP FOR OPERATION AND MAINTENANCE OF FOGGER Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask METHOD OF ANALYSIS FOR SODIUM HYDROXIDE : PHARMACEUTICAL Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask PHARMACEUTICAL GUIDELINES : TOTAL PHARMACEUTICAL SOLUTIONSOPSQUALITY CONTROLQUALITY ASSURANCEMICROBIOLOGYPRODUCTIONVALIDATION A blog about pharmaceutical quality control, quality assurance, microbiology, production and regulatory updates provided by regulatoryagencies.
PHARMA SOPS : PHARMACEUTICAL GUIDELINESPRODUCTIONDOCUMENTSSOPS FOR QUALITY CONTROLABOUT ANKUR CHOUDHARY Standard Operating Procedures (SOPs) is a written procedure for any process or system that is followed during the operation of any systemor equipment.
SOPS FOR STORES/ WAREHOUSE : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for stores/ warehouse department in pharmaceutical manufacturing plant. SOPS FOR MICROBIOLOGY : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for microbiology department (sterile and non-sterile) in pharmaceutical products manufacturing facility. ABOUT ANKUR CHOUDHARY : PHARMACEUTICAL GUIDELINES Ankur Choudhary is a professional pharmaceutical blogger from India having rich experience in the pharmaceutical field. After completion of his Masters of Science in Microbiology in 2002 from Gurukul Kangri University, he started his job in the pharmaceutical industry. GOOD DOCUMENTATION PRACTICES (GDP) These are the articles on good documentation practices in a pharmaceutical manufacturing facility, those are helpful to new as well as experienced pharmaceutical professionals PHARMACEUTICAL GUIDELINES : TOTAL PHARMACEUTICAL SOLUTIONSOPSQUALITY CONTROLQUALITY ASSURANCEMICROBIOLOGYPRODUCTIONVALIDATION A blog about pharmaceutical quality control, quality assurance, microbiology, production and regulatory updates provided by regulatoryagencies.
PHARMA SOPS : PHARMACEUTICAL GUIDELINESPRODUCTIONDOCUMENTSSOPS FOR QUALITY CONTROLABOUT ANKUR CHOUDHARY Standard Operating Procedures (SOPs) is a written procedure for any process or system that is followed during the operation of any systemor equipment.
SOPS FOR STORES/ WAREHOUSE : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for stores/ warehouse department in pharmaceutical manufacturing plant. SOPS FOR MICROBIOLOGY : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for microbiology department (sterile and non-sterile) in pharmaceutical products manufacturing facility. ABOUT ANKUR CHOUDHARY : PHARMACEUTICAL GUIDELINES Ankur Choudhary is a professional pharmaceutical blogger from India having rich experience in the pharmaceutical field. After completion of his Masters of Science in Microbiology in 2002 from Gurukul Kangri University, he started his job in the pharmaceutical industry. GOOD DOCUMENTATION PRACTICES (GDP) These are the articles on good documentation practices in a pharmaceutical manufacturing facility, those are helpful to new as well as experienced pharmaceutical professionals COVID-19 SOP FOR HOME : PHARMACEUTICAL GUIDELINES 1.0 Objective: To lay down the procedure for prevention from COVID-19 at home. 2.0 Scope: This procedure is applicable to the home of everyone. 3.0 Responsibility: Every member of the home. 4.0 Accountability: Housewife in the home. 5.0 Procedure: 5.1 Visits to the Market 5.1.1 Always wear a triple layer /N95 nose mask or use face cover when you go out of your home. SOPS FOR QUALITY CONTROL : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for Quality Control laboratories in pharmaceutical products manufacturing facilities. SOP FOR DATA INTEGRITY : PHARMACEUTICAL GUIDELINES Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask CHECKLIST FOR AUDIT IN QUALITY CONTROL : PHARMACEUTICAL Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask SOP FOR WATER BATH : PHARMACEUTICAL GUIDELINES 1.0 OBJECTIVE To describe the procedure for Operation and calibration of the water bath. 2.0 SCOPE This SOP is applicable for Operation and calibration of the water bath. SOP FOR PERSONNEL GOWNING QUALIFICATION : PHARMACEUTICAL 5.3.1.1 Personal Monitoring by Contact plate (RODAC) technique. The Personnel shall enter in the aseptic area along with the microbiologist; Personnel and Microbiologist shall enter into the aseptic area as per current SOP of entry and exit to the Microbiology and Production area. CHECKLIST FOR AUDIT IN WAREHOUSE : PHARMACEUTICAL GUIDELINES Checklist to prepare for audit in warehouse/ stores. 1. Whether the storage area is adequately designed for better storage conditions? (i.e. temperature, light, humidity & cleanliness). CAUSES AND REMEDIES OF LAMINATION IN TABLET MANUFACTURING An ideal tablet should be free from any visual defects as well as the functional defects. Despite the advancements and innovations in the manufacturing of tablets, the problems that are often encountered in the production have not decreased but instead increased. METHOD OF ANALYSIS FOR ASCORBIC ACID : PHARMACEUTICAL Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask DIFFERENCE BETWEEN RECALL AND MOCK RECALL : PHARMACEUTICAL Difference between Recall and Mock Recall Recall and mock recall procedures for pharmaceuticals are different from each other. One is used to get back the marketed PHARMACEUTICAL GUIDELINES : TOTAL PHARMACEUTICAL SOLUTIONSOPSQUALITY CONTROLQUALITY ASSURANCEMICROBIOLOGYPRODUCTIONVALIDATION A blog about pharmaceutical quality control, quality assurance, microbiology, production and regulatory updates provided by regulatoryagencies.
PHARMA SOPS : PHARMACEUTICAL GUIDELINESPRODUCTIONDOCUMENTSSOPS FOR QUALITY CONTROLABOUT ANKUR CHOUDHARY Standard Operating Procedures (SOPs) is a written procedure for any process or system that is followed during the operation of any systemor equipment.
SOPS FOR STORES/ WAREHOUSE : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for stores/ warehouse department in pharmaceutical manufacturing plant. SOP FOR DISINFECTANT EFFICACY TEST : PHARMACEUTICAL GUIDELINES Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask FAULT TREE ANALYSIS FOR INVESTIGATION : PHARMACEUTICAL Fault Tree Analysis for Investigation You will find many articles on fault tree analysis but this is actual method with example by which you can actually prepare a fault tree diagram for the events or problems you found in pharmaceutical manufacturing industry. SOP FOR PROCESS VALIDATION : PHARMACEUTICAL GUIDELINES 1.0 OBJECTIVE The purpose of this SOP is to lay down the minimum requirements for validation or revalidation of manufacturing processes applicable to marketed drug products in order to provide documented evidence that each specific process will consistently yield a product meeting all quality and design specifications. SOP FOR PERSONNEL GOWNING QUALIFICATION : PHARMACEUTICAL 5.3.1.1 Personal Monitoring by Contact plate (RODAC) technique. The Personnel shall enter in the aseptic area along with the microbiologist; Personnel and Microbiologist shall enter into the aseptic area as per current SOP of entry and exit to the Microbiology and Production area. REVALIDATION OF EQUIPMENT AND PROCESS IN PHARMACEUTICALS Revalidation in the pharmaceutical industry is very important as it helps to maintain the validated status of the equipment, plant, manufacturing process as well as the computer systems. This procedure is necessary for periodic checking of the validation results according to the revalidation period. CLIMATIC ZONES FOR STABILITY STUDIES : PHARMACEUTICAL The climate is different in all the countries in the world. Stability studies of the pharmaceutical drug should be done according to the climatic conditions of the country. According to the ICH guidelines for stability studies, the climate of the world is divided into fivedifferent zones.
OCCUPATIONAL EXPOSURE BANDS (OEBS) FOR CHEMICALS Occupational exposure bands are measures put in place to categorize chemicals so that the health of the worker is not compromised. This is because Active Pharmaceutical Ingredients can have serious and adverse effects on the worker when they become lowly airborne. PHARMACEUTICAL GUIDELINES : TOTAL PHARMACEUTICAL SOLUTIONSOPSQUALITY CONTROLQUALITY ASSURANCEMICROBIOLOGYPRODUCTIONVALIDATION A blog about pharmaceutical quality control, quality assurance, microbiology, production and regulatory updates provided by regulatoryagencies.
PHARMA SOPS : PHARMACEUTICAL GUIDELINESPRODUCTIONDOCUMENTSSOPS FOR QUALITY CONTROLABOUT ANKUR CHOUDHARY Standard Operating Procedures (SOPs) is a written procedure for any process or system that is followed during the operation of any systemor equipment.
SOPS FOR STORES/ WAREHOUSE : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for stores/ warehouse department in pharmaceutical manufacturing plant. SOP FOR DISINFECTANT EFFICACY TEST : PHARMACEUTICAL GUIDELINES Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask FAULT TREE ANALYSIS FOR INVESTIGATION : PHARMACEUTICAL Fault Tree Analysis for Investigation You will find many articles on fault tree analysis but this is actual method with example by which you can actually prepare a fault tree diagram for the events or problems you found in pharmaceutical manufacturing industry. SOP FOR PROCESS VALIDATION : PHARMACEUTICAL GUIDELINES 1.0 OBJECTIVE The purpose of this SOP is to lay down the minimum requirements for validation or revalidation of manufacturing processes applicable to marketed drug products in order to provide documented evidence that each specific process will consistently yield a product meeting all quality and design specifications. SOP FOR PERSONNEL GOWNING QUALIFICATION : PHARMACEUTICAL 5.3.1.1 Personal Monitoring by Contact plate (RODAC) technique. The Personnel shall enter in the aseptic area along with the microbiologist; Personnel and Microbiologist shall enter into the aseptic area as per current SOP of entry and exit to the Microbiology and Production area. REVALIDATION OF EQUIPMENT AND PROCESS IN PHARMACEUTICALS Revalidation in the pharmaceutical industry is very important as it helps to maintain the validated status of the equipment, plant, manufacturing process as well as the computer systems. This procedure is necessary for periodic checking of the validation results according to the revalidation period. CLIMATIC ZONES FOR STABILITY STUDIES : PHARMACEUTICAL The climate is different in all the countries in the world. Stability studies of the pharmaceutical drug should be done according to the climatic conditions of the country. According to the ICH guidelines for stability studies, the climate of the world is divided into fivedifferent zones.
OCCUPATIONAL EXPOSURE BANDS (OEBS) FOR CHEMICALS Occupational exposure bands are measures put in place to categorize chemicals so that the health of the worker is not compromised. This is because Active Pharmaceutical Ingredients can have serious and adverse effects on the worker when they become lowly airborne. SOPS FOR STORES/ WAREHOUSE : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for stores/ warehouse department in pharmaceutical manufacturing plant. QUALITY ASSURANCE : PHARMACEUTICAL GUIDELINES Following are the articles related to pharmaceutical quality assurance and quality management system for pharmaceutical industry those arehelpful for new as
ORAL LIQUID PHARMACEUTICAL DOSAGE FORMS : PHARMACEUTICAL Oral Emulsion is an oral liquid that contains one or more active ingredients that are unstable in the water phase and is stabilized oil-in-water dispersions; either or WORKING PRINCIPLE OF PH METER : PHARMACEUTICAL GUIDELINES A pH meter is used to determine the acidity or alkalinity of the solution. pH is the concentration of hydrogen ions in the solution. A solution containing more H + ions remains acidic while the solution containing more OH-ions remains alkaline. pH value of solutions rangesfrom 1 to 14.
SOP FOR ACCEPTABLE QUALITY LEVEL (AQL) : PHARMACEUTICAL 5.5.1 If the no. of major /minor reject is at higher side. 5.5.2 If the results of AQL does not comply with the accept level. 5.6 If the cumulative total of a different defective sample in critical / major / minor category exceeds the stated ‘accept’ level, follow instruction 5.5 and again carry out AQL test as per procedure. ROLE OF REGULATORY AFFAIRS IN PHARMACEUTICALS Regulatory affairs in pharmaceuticals are like vehicle inspectors in the automotive industry. They assess and perform quality checks to ensure that the medicinal drugs, veterinary drugs, and nutritional supplements rolled out by the pharmaceutical industry are safe and effective for the consumers to use. SOP FOR PASSWORD POLICY AND DATA BACKUP AND STORAGE FOR 5.3.1 Yearly Backup: Upon completion of the year, analytical data of previous year shall be backed-up from IT server in pre-numbered tape in duplicate, Head IT shall be the custodian for the backup tapes. 5.3.1.1 Tolerance of the yearly backup data shall be ten working days after due date of yearly back-up. 5.3.1.2 Necessary entry shall be made in the yearly backup register. SOP FOR HANDLING OF REJECTED RAW MATERIAL : PHARMACEUTICAL 5.2 Material reject during testing by Q.C. department 5.2.1 If the material is rejected by Q.C. department during testing, store person shall ask rejection note from Q.C. department and send it to purchase department for information. DIFFERENCE BETWEEN RECALL AND MOCK RECALL : PHARMACEUTICAL Difference between Recall and Mock Recall Recall and mock recall procedures for pharmaceuticals are different from each other. One is used to get back the marketed DIFFERENCE BETWEEN STERILE AND PYROGEN FREE That being said, you should easily understand the difference between being sterile and being pyrogen-free as explained here. The process of sterilization is the killing, removal or deactivation of living microorganisms from equipment, solutions or pharmaceutical vials. PHARMACEUTICAL GUIDELINES : TOTAL PHARMACEUTICAL SOLUTIONSOPSQUALITY CONTROLQUALITY ASSURANCEMICROBIOLOGYPRODUCTIONVALIDATION A blog about pharmaceutical quality control, quality assurance, microbiology, production and regulatory updates provided by regulatoryagencies.
PHARMA SOPS : PHARMACEUTICAL GUIDELINESPRODUCTIONDOCUMENTSSOPS FOR QUALITY CONTROLABOUT ANKUR CHOUDHARY Standard Operating Procedures (SOPs) is a written procedure for any process or system that is followed during the operation of any systemor equipment.
SOPS FOR STORES/ WAREHOUSE : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for stores/ warehouse department in pharmaceutical manufacturing plant. SOP FOR DISINFECTANT EFFICACY TEST : PHARMACEUTICAL GUIDELINES Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask FAULT TREE ANALYSIS FOR INVESTIGATION : PHARMACEUTICALFTA RECEIVERS FOR NORTH AMERICAFTA SATELLITE SYSTEMS FOR SALEAPPLIED BEHAVIOR ANALYSIS MANUAL PDFARMY COST ANALYSIS MANUALARMY ECONOMIC ANALYSIS MANUALFIRE SAFETY ANALYSIS MANUAL Fault Tree Analysis for Investigation You will find many articles on fault tree analysis but this is actual method with example by which you can actually prepare a fault tree diagram for the events or problems you found in pharmaceutical manufacturing industry. SOP FOR PROCESS VALIDATION : PHARMACEUTICAL GUIDELINES 1.0 OBJECTIVE The purpose of this SOP is to lay down the minimum requirements for validation or revalidation of manufacturing processes applicable to marketed drug products in order to provide documented evidence that each specific process will consistently yield a product meeting all quality and design specifications. SOP FOR PERSONNEL GOWNING QUALIFICATION : PHARMACEUTICAL 5.3.1.1 Personal Monitoring by Contact plate (RODAC) technique. The Personnel shall enter in the aseptic area along with the microbiologist; Personnel and Microbiologist shall enter into the aseptic area as per current SOP of entry and exit to the Microbiology and Production area. REVALIDATION OF EQUIPMENT AND PROCESS IN PHARMACEUTICALSEQUIPMENTVALIDATION PROCESS
Revalidation in the pharmaceutical industry is very important as it helps to maintain the validated status of the equipment, plant, manufacturing process as well as the computer systems. This procedure is necessary for periodic checking of the validation results according to the revalidation period. PHARMACEUTICAL GUIDELINES : TOTAL PHARMACEUTICAL SOLUTIONSOPSQUALITY CONTROLQUALITY ASSURANCEMICROBIOLOGYPRODUCTIONVALIDATION A blog about pharmaceutical quality control, quality assurance, microbiology, production and regulatory updates provided by regulatoryagencies.
PHARMA SOPS : PHARMACEUTICAL GUIDELINESPRODUCTIONDOCUMENTSSOPS FOR QUALITY CONTROLABOUT ANKUR CHOUDHARY Standard Operating Procedures (SOPs) is a written procedure for any process or system that is followed during the operation of any systemor equipment.
SOPS FOR STORES/ WAREHOUSE : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for stores/ warehouse department in pharmaceutical manufacturing plant. SOP FOR DISINFECTANT EFFICACY TEST : PHARMACEUTICAL GUIDELINES Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips..moc.enilediugamrahp@ofni :liamE Need Help: Ask FAULT TREE ANALYSIS FOR INVESTIGATION : PHARMACEUTICALFTA RECEIVERS FOR NORTH AMERICAFTA SATELLITE SYSTEMS FOR SALEAPPLIED BEHAVIOR ANALYSIS MANUAL PDFARMY COST ANALYSIS MANUALARMY ECONOMIC ANALYSIS MANUALFIRE SAFETY ANALYSIS MANUAL Fault Tree Analysis for Investigation You will find many articles on fault tree analysis but this is actual method with example by which you can actually prepare a fault tree diagram for the events or problems you found in pharmaceutical manufacturing industry. SOP FOR PROCESS VALIDATION : PHARMACEUTICAL GUIDELINES 1.0 OBJECTIVE The purpose of this SOP is to lay down the minimum requirements for validation or revalidation of manufacturing processes applicable to marketed drug products in order to provide documented evidence that each specific process will consistently yield a product meeting all quality and design specifications. SOP FOR PERSONNEL GOWNING QUALIFICATION : PHARMACEUTICAL 5.3.1.1 Personal Monitoring by Contact plate (RODAC) technique. The Personnel shall enter in the aseptic area along with the microbiologist; Personnel and Microbiologist shall enter into the aseptic area as per current SOP of entry and exit to the Microbiology and Production area. REVALIDATION OF EQUIPMENT AND PROCESS IN PHARMACEUTICALSEQUIPMENTVALIDATION PROCESS
Revalidation in the pharmaceutical industry is very important as it helps to maintain the validated status of the equipment, plant, manufacturing process as well as the computer systems. This procedure is necessary for periodic checking of the validation results according to the revalidation period. CLIMATIC ZONES FOR STABILITY STUDIES : PHARMACEUTICAL The climate is different in all the countries in the world. Stability studies of the pharmaceutical drug should be done according to the climatic conditions of the country. According to the ICH guidelines for stability studies, the climate of the world is divided into fivedifferent zones.
OCCUPATIONAL EXPOSURE BANDS (OEBS) FOR CHEMICALS Occupational exposure bands are measures put in place to categorize chemicals so that the health of the worker is not compromised. This is because Active Pharmaceutical Ingredients can have serious and adverse effects on the worker when they become lowly airborne. SOPS FOR STORES/ WAREHOUSE : PHARMACEUTICAL GUIDELINES List of Standard Operating Procedures (SOPs) for stores/ warehouse department in pharmaceutical manufacturing plant. QUALITY ASSURANCE : PHARMACEUTICAL GUIDELINES Following are the articles related to pharmaceutical quality assurance and quality management system for pharmaceutical industry those arehelpful for new as
ORAL LIQUID PHARMACEUTICAL DOSAGE FORMS : PHARMACEUTICAL Oral Emulsion is an oral liquid that contains one or more active ingredients that are unstable in the water phase and is stabilized oil-in-water dispersions; either or SOP FOR ACCEPTABLE QUALITY LEVEL (AQL) : PHARMACEUTICAL 5.5.1 If the no. of major /minor reject is at higher side. 5.5.2 If the results of AQL does not comply with the accept level. 5.6 If the cumulative total of a different defective sample in critical / major / minor category exceeds the stated ‘accept’ level, follow instruction 5.5 and again carry out AQL test as per procedure. WORKING PRINCIPLE OF PH METER : PHARMACEUTICAL GUIDELINES A pH meter is used to determine the acidity or alkalinity of the solution. pH is the concentration of hydrogen ions in the solution. A solution containing more H + ions remains acidic while the solution containing more OH-ions remains alkaline. pH value of solutions rangesfrom 1 to 14.
ROLE OF REGULATORY AFFAIRS IN PHARMACEUTICALS Regulatory affairs in pharmaceuticals are like vehicle inspectors in the automotive industry. They assess and perform quality checks to ensure that the medicinal drugs, veterinary drugs, and nutritional supplements rolled out by the pharmaceutical industry are safe and effective for the consumers to use. SOP FOR PASSWORD POLICY AND DATA BACKUP AND STORAGE FOR 5.3.1 Yearly Backup: Upon completion of the year, analytical data of previous year shall be backed-up from IT server in pre-numbered tape in duplicate, Head IT shall be the custodian for the backup tapes. 5.3.1.1 Tolerance of the yearly backup data shall be ten working days after due date of yearly back-up. 5.3.1.2 Necessary entry shall be made in the yearly backup register. SOP FOR HANDLING OF REJECTED RAW MATERIAL : PHARMACEUTICAL 5.2 Material reject during testing by Q.C. department 5.2.1 If the material is rejected by Q.C. department during testing, store person shall ask rejection note from Q.C. department and send it to purchase department for information. DIFFERENCE BETWEEN RECALL AND MOCK RECALL : PHARMACEUTICAL Difference between Recall and Mock Recall Recall and mock recall procedures for pharmaceuticals are different from each other. One is used to get back the marketed DIFFERENCE BETWEEN STERILE AND PYROGEN FREE That being said, you should easily understand the difference between being sterile and being pyrogen-free as explained here. The process of sterilization is the killing, removal or deactivation of living microorganisms from equipment, solutions or pharmaceutical vials. Pharmaceutical Guidelines : Total Pharmaceutical Solution PHARMACEUTICAL GUIDELINES* About
* Forum
* Store
* Videos
* Research
* Advertise
* Affiliate
* Contact Us
* App
* Books
* Disclaimer
* Privacy
__ __
__
__
__
__
__
Editable Pharmaceutical Documents in MS-Word FormatView
Join Log In
8
.
×
search
Home Quality ControlQuality
Assurance
Microbiology
Production SOPs
Validation
GMP
Audit
Ask Question
Documents
__
Custom Search
COVID-19 SOP FOR HOME__May 8, 2020_ _SOP
__ No comments
1.0 OBJECTIVE: To lay down the procedure for prevention from COVID-19at home.
2.0 SCOPE: This procedure is applicable to the home of everyone. 3.0 RESPONSIBILITY: Every member of the home. 4.0 ACCOUNTABILITY: Housewife in the home.____
__
__
Full Article
__2386
__Share
__Tweet
__Share
PREVENTION OF MICROBIAL CONTAMINATION IN MANUFACTURING __May 4, 2020_ _Microbiology,
Production ,
Sterile __ 3
comments
The quality and safety of pharmaceutical products should be a key concern to any manufacturer in order to take care of clients consuming the product as well as maintaining their brand name in the market. Therefore to prevent microbial contamination in pharmaceutical products, there are some key measures or considerations that a manufacturer needs to take care of.____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
CRITICAL AND NON-CRITICAL AREAS IN PHARMACEUTICAL MANUFACTURING __Apr 27, 2020_ _Production, Sterile
__ No comments
Appropriate design, positioning and use of critical and non-critical areas in the pharmaceutical manufacturing process are among the key prerequisites for success in this industry. Critical areas include all areas in which any kind of sterile product (including both drugs and equipment) must be exposed to the sterile environment and where activities including sterilization, sterile filling and c…____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
DIFFERENT TYPES OF HPLC DETECTORS __Apr 19, 2020_ _HPLC, Quality Control
__ 2
comments
HPLC detectors are used in the detection of the solute present in the eluent coming from the HPLC column. They are capable of determining the identity and concentration of eluting compounds in the mobile phase. There are specific detectors which respond to a specific compound and their response is not dependent on mobile phasecomposition.
____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
CONCEPT OF GXP IN PHARMACEUTICALS __Apr 12, 2020_ _GDP, GLP
, GMP
__ 1 comment
One of the biggest concerns that the pharmaceutical industry constantly attempts to address is the safety of its products. GxP is a collection of regulations that aim to resolve this matter in a systematic and wholesome manner. The concept of GxP requirements in Pharmaceuticals was established by the United States Food and Drug Administration. The term itself encircles many differentregulations…
____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
CRITERIA FOR SELECTION OF CLEAN ROOM GARMENTS IN PHARMACEUTICALS__Apr 5, 2020_ _GMP
, Production
, Sterile
__ 3 comments
A clean room in the pharmaceutical industry is a specialized place that has very limited contaminants such as air particulates and chemicals so as to ensure the quality of the products produced is not only achieved but also maintained. In order to achieve such a sterile environment, the products, as well as clothing that enter the GMP clean room, should be of the highest quality to prevent bringi…____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
BEST WEIGHING PRACTICES IN PHARMACEUTICALS __Mar 29, 2020_ _GLP, GMP
__ 1 comment
It has always been a great challenge for many people when it comes to adopting and using the best weighing practices in pharmaceutical industries. This is simply because electronic balances that are used may create the wrong impression sometimes that they are offering guaranteed measurement precision. That's why below, we have compiled the best practices to help you as an individual or organi…____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
REQUIREMENT OF ALARM SYSTEM IN CRITICAL EQUIPMENTS __Mar 22, 2020_ _GLP, GMP
, Regulatory
__ No
comments
The general function of an alarm is to warn about any critical condition as a life-threatening danger or any critical environmental condition like building fire alarm etc. But in the pharmaceutical manufacturing facility, the requirement of audible alarm in critical equipment has its great importance because the change in temperature can affect the pharmaceutical product quality or it can alter …____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
PROTECTIVE GEARS USED IN PHARMACEUTICAL STERILE AREAS __Mar 15, 2020_ _Microbiology,
Production ,
Sterile __ No
comments
In the health-related area, laboratories need to follow strict measures in order to keep everything flowing. Not only to protect the workers from possible hazards but to protect the patients from possible anomalies in the manipulated substances. In this article, we will tell you more about the laboratory protective gear in the pharmaceutical sterile area and how to use it.____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
LUX AND LIGHT INTENSITY FOR PHARMACEUTICAL AREAS__Mar 8, 2020_ _GLP
, GMP
__ 6 comments
Sufficient light is necessary at the workplace to get better work output. Less lighting in working area can result in errors in different ways. None should experience eye-strain during his work.____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
IMPORTANCE OF BLEND UNIFORMITY IN MANUFACTURING PROCESS__Mar 1, 2020_ _GMP
, Non-sterile
, Production
__ No
comments
Blend uniformity is an important factor in pharmaceutical manufacturing. A poor uniformity of the blend can cause the rejection of the product that can lead to the loss of revenue.____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
HANDLING STATIC CHARGE IN PHARMACEUTICAL MANUFACTURING __Feb 23, 2020_ _GMP, Production
, Quality
Assurance
__ 6
comments
Static charge is the electric current developed by the rubbing of moving parts of equipment or contact and separation of material particles. It is generated in different pharmaceutical manufacturing equipment during processing. Sometimes it is generated by the continuous flow of the powder on the equipment surface.____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
FISHBONE TOOL OF INVESTIGATION IN PHARMACEUTICALS __Feb 16, 2020_ _Audit, GMP
, Quality Assurance
__ 4
comments
Fishbone diagrams, also known as Ishikawa fishbone diagrams, is a visual form of cause and effect diagram which can help analyze the root causes of a problem. It allows the audience to brainstorm the reasons which might otherwise be directly ignored. These causal diagrams have been in use since 1968 to find root-cause analysis of aspecific event.
____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
DIFFERENT TYPES OF HPLC COLUMNS USED IN ANALYSIS__Feb 9, 2020_ _GLP
, HPLC
, Quality Control
__ 8
comments
Columns are the main component in HPLC because the column is responsible for the separation of the sample components. The sample passes through the column with the mobile phase and separates in its components when it comes out from the column.____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
PLANNING AND EXECUTION OF INTERNAL AUDITS IN PHARMACEUTICALS __Feb 2, 2020_ _Audit, GLP
, GMP
__ 3 comments
In any type of audit, the first and most important part is making a plan. In order to make the execution of audit of pharmaceutical effective and efficient, a good audit plan is compulsory. Internal Audits can be a valuable tool for any company for information collection and assessment of daily performance.____
__
__
__
Full Article
__2386
__Share
__Tweet
__Share
ABOUT THE AUTHOR
------------------------- ◉ ONLINE Ankur Choudharyis experienced in
pharmaceutical, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Email: INFO@PHARMAGUIDELINE.COMPOPULAR CATEGORIES
QA SOPs
QC
SOPs
Micro SOPs
HVAC
Production SOPs
Stores
SOPs
Checklists
Maintenance SOPs
HPLC
Sterile
GLP
Validation ProtocolsWater System
GDP
Regulatory
Maintenance
Calibration
Warning Letters
Download COVID-19 SOP for Home FOLLOW PHARMAGUIDELINE__Like
__Follow
__Follow
__Follow
__Follow
__Install
__Join
GET FREE UPDATES
__Subscribe
DOCUMENTS
PHARMACEUTICAL DOCUMENTS ------------------------- ------------------------- ------------------------- Editable Pharmaceutical Documents in MS-Word Format. Ready to use SOPs, Protocols, Master Plans, Manuals and more...View
_adsbypg_
DISCUSSION - LATEST TOPICS * Please provide me sample formates for DMF I, II, III, IV and V* GPT of DENA Agar
* Give me one simple bulk drugs(raw, api) and finished productsprocedure
* Storage and transport of TTSPPs ( Time and Temperature Sensitive pharmaceutical products) * Data integrity in document * Deviation and incedent * Pharmaceutical Equipment's Capacity * D-value requirement * Binder change from hydroalcoholic to aqueous * Rinsing membrane filter * Differences between GC and HPLC * Drug and cosmotic ruleShow All
❭❭ _Pharmaguideline Forum_ GET APP FOR NEWS UPDATES Pharmaceutical Updates ------------------------- ------------------------- ------------------------- ✔ Worldwide Regulatory Updates ✔ Pharmaceutical News Updates ✔ Interview Questions and Answers ✔ All Guidelines in One PlaceInstall
*
*
__ __
__
__
__
__
*
Copyright © 2008-2020 Pharmaceutical GuidelinesSetup ❘ Terms of
Use ❘ FAQ
__
Details
Copyright © 2024 ArchiveBay.com. All rights reserved. Terms of Use | Privacy Policy | DMCA | 2021 | Feedback | Advertising | RSS 2.0