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CODES & GUIDELINES
Codes & Guidelines. PhRMA represents the nation’s leading biopharmaceutical research companies. Our success in developing and delivering medicines to help patients live longer and healthier lives depends on ethical relationships and behavior. Browse key Codes and PHRMA’S EQUITY INITIATIVE PhRMA CAREs Grant: Addressing Racial Disparities in Medication Utilization and Adherence. In 2019, PhRMA established the Health Equity Roundtable with the goal of improving health outcomes by addressing inequities in care. As part of the Health Equity Roundtable, PhRMA is offering funding opportunities to spur ideas for practical interventions MEDICINES IN DEVELOPMENT Medicines in Development for Antimicrobial Resistance 2021 Report. Today, more than 1,300 medicines and vaccines for various cancers are currently in development by innovative biopharmaceutical research companies, all of which are in clinical trials or awaiting review by CLINICAL TRIAL DIVERSITY Clinical trial diversity helps to ensure we have medications that are suited to reflect and treat the intended treatment population. That’s why our entire industry came together to develop and voluntarily adopt principles on closing the diversity gaps. Understanding the challenges of PHRMA STATEMENT ON HOUSE LEADERSHIP’S “PARTISAN” DRUG PhRMA Statement on House Leadership’s “Partisan” Drug Pricing Proposal. WASHINGTON, D.C. (April 22, 2021) – Pharmaceutical Research and Manufacturers of America president and CEO Stephen J. Ubl issued the following statement today after House Democratic leaders released their partisan drug pricing proposal: “The American peoplewant
FOLLOW THE DOLLAR REPORT Follow the Dollar Report. This paper provides a high-level explanation of the financial flows that occur as brand medicines move through the supply chain for retail, mail-order and specialty drugs. Download the Executive Summary. Download the Report. -. CLINICAL TRIAL DATA TRANSPARENCY Clinical trial data transparency has multiple elements, all of which are aimed at improving access to clinical trial information in order to inform medical decision-making, advance scientific discovery and accelerate development of new treatments to benefit patients.DOWNLOAD. -.
BIOPHARMACEUTICAL DIGITAL HEALTH LEXICON Digital health is transforming nearly every aspect of our health care system, improving efficiency, expanding access to treatments and technologies, and ushering in increased development of personalized medicine. One of the foundational elements of a modern digital R&D regulatory framework is a common lexicon and understanding of key terms to orient stakeholders and facilitate CODE ON INTERACTIONS Therefore, PhRMA adopts this updated and enhanced voluntary Code on relationships with U.S. health care professionals. This Code reflects and builds upon the standards and principles set forth in INNOVATIVE CONTRACTING: OPPORTUNITIES AND CHALLENGES INNOVATIVE CONTRACTS CAN BE BENEFICIAL TO PATIENTS AND LOWER OUT-OF-POCKET COSTS WHILE PROVIDING SAVINGS FOR THE HEALTH SYSTEM. 1 Avalere. More than Half of Health Plans Use Outcomes-Based Contracts.CODES & GUIDELINES
Codes & Guidelines. PhRMA represents the nation’s leading biopharmaceutical research companies. Our success in developing and delivering medicines to help patients live longer and healthier lives depends on ethical relationships and behavior. Browse key Codes and PHRMA’S EQUITY INITIATIVE PhRMA CAREs Grant: Addressing Racial Disparities in Medication Utilization and Adherence. In 2019, PhRMA established the Health Equity Roundtable with the goal of improving health outcomes by addressing inequities in care. As part of the Health Equity Roundtable, PhRMA is offering funding opportunities to spur ideas for practical interventions MEDICINES IN DEVELOPMENT Medicines in Development for Antimicrobial Resistance 2021 Report. Today, more than 1,300 medicines and vaccines for various cancers are currently in development by innovative biopharmaceutical research companies, all of which are in clinical trials or awaiting review by CLINICAL TRIAL DIVERSITY Clinical trial diversity helps to ensure we have medications that are suited to reflect and treat the intended treatment population. That’s why our entire industry came together to develop and voluntarily adopt principles on closing the diversity gaps. Understanding the challenges of PHRMA STATEMENT ON HOUSE LEADERSHIP’S “PARTISAN” DRUG PhRMA Statement on House Leadership’s “Partisan” Drug Pricing Proposal. WASHINGTON, D.C. (April 22, 2021) – Pharmaceutical Research and Manufacturers of America president and CEO Stephen J. Ubl issued the following statement today after House Democratic leaders released their partisan drug pricing proposal: “The American peoplewant
FOLLOW THE DOLLAR REPORT Follow the Dollar Report. This paper provides a high-level explanation of the financial flows that occur as brand medicines move through the supply chain for retail, mail-order and specialty drugs. Download the Executive Summary. Download the Report. -. CLINICAL TRIAL DATA TRANSPARENCY Clinical trial data transparency has multiple elements, all of which are aimed at improving access to clinical trial information in order to inform medical decision-making, advance scientific discovery and accelerate development of new treatments to benefit patients.DOWNLOAD. -.
BIOPHARMACEUTICAL DIGITAL HEALTH LEXICON Digital health is transforming nearly every aspect of our health care system, improving efficiency, expanding access to treatments and technologies, and ushering in increased development of personalized medicine. One of the foundational elements of a modern digital R&D regulatory framework is a common lexicon and understanding of key terms to orient stakeholders and facilitate CODE ON INTERACTIONS Therefore, PhRMA adopts this updated and enhanced voluntary Code on relationships with U.S. health care professionals. This Code reflects and builds upon the standards and principles set forth in INNOVATIVE CONTRACTING: OPPORTUNITIES AND CHALLENGES INNOVATIVE CONTRACTS CAN BE BENEFICIAL TO PATIENTS AND LOWER OUT-OF-POCKET COSTS WHILE PROVIDING SAVINGS FOR THE HEALTH SYSTEM. 1 Avalere. More than Half of Health Plans Use Outcomes-Based Contracts.PHRMA ORG | PHRMA
Working Together to Fight COVID-19. The Pharmaceutical Research and Manufacturers of America, PhRMA, represents the country’s leading biopharmaceutical researchers MEDICINES IN DEVELOPMENT Medicines in Development for Antimicrobial Resistance 2021 Report. Today, more than 1,300 medicines and vaccines for various cancers are currently in development by innovative biopharmaceutical research companies, all of which are in clinical trials or awaiting review by GET HELP WITH YOUR PRESCRIPTIONS Navigating the complexities of today’s health care system can be confusing and overwhelming, but it doesn’t have to be. America’s biopharmaceutical research companies that make up PhRMA have partnered with health care providers, pharmacists, patient advocacy organizations and community groups to help patients afford their medicines by creating the Medicine Assistance Tool (MAT). PHRMA STATEMENT ON HOUSE LEADERSHIP’S “PARTISAN” DRUG WASHINGTON, D.C. (April 22, 2021) – Pharmaceutical Research and Manufacturers of America president and CEO Stephen J. Ubl issued the following statement today after House Democratic leaders released their partisan drug pricing proposal: “The American people want to end the pandemic, get the economy back on track and make health care more affordable and predictable.ACCESS TO MEDICINES
Patient access to the medicines they need is critical both for individuals and for our health care system more broadly. In the United States, patients can access medicines a number of ways, including through employer-sponsored health plan, a health insurance exchange plan or a program like Medicare or Medicaid. Today, Americans havefaster
COMING TOGETHER TO FIGHT COVID-19: A CONVERSATION WITH Stephen J. Ubl Stephen J. Ubl is president and chief executive officer of PhRMA. Mr. Ubl leads PhRMA’s work preserving and strengthening a health care and economic environment that encourages medical innovation, new drug discovery and access to life-saving medicines. THE DANGERS OF H.R. 3 A BETTER WAY w hite We can achieve those goals, but the drug pricing plan known as H.R. 3 is not the answer. If implemented, it could have devastating consequences for patients’ access to medicines, future innovation and American jobs. HOW RESEARCH EVOLVES AND BRINGS NEW HOPE TO PATIENTS Stephen J. Ubl Stephen J. Ubl is president and chief executive officer of PhRMA. Mr. Ubl leads PhRMA’s work preserving and strengthening a health care and economic environment that encourages medical innovation, new drug discovery and access to life-saving medicines. OBTAINING A PATENT REQUIRES PASSING THROUGH A ROBUST AND Obtaining a Patent Requires Passing Through a Robust and Thorough Process INVENTION A patent starts with an idea that can be described in a patent application, which BIOPHARMACEUTICAL RESEARCH & DEVELOPMENT phase i phase ii phase iii phase iv ind submitted tens number of volunteers hundreds thousands nda/bla submitted fda approval the biopharmaceutical research and development processCODES & GUIDELINES
Codes & Guidelines. PhRMA represents the nation’s leading biopharmaceutical research companies. Our success in developing and delivering medicines to help patients live longer and healthier lives depends on ethical relationships and behavior. Browse key Codes and PHRMA’S EQUITY INITIATIVE PhRMA CAREs Grant: Addressing Racial Disparities in Medication Utilization and Adherence. In 2019, PhRMA established the Health Equity Roundtable with the goal of improving health outcomes by addressing inequities in care. As part of the Health Equity Roundtable, PhRMA is offering funding opportunities to spur ideas for practical interventions MEDICINES IN DEVELOPMENT Medicines in Development for Antimicrobial Resistance 2021 Report. Today, more than 1,300 medicines and vaccines for various cancers are currently in development by innovative biopharmaceutical research companies, all of which are in clinical trials or awaiting review by CLINICAL TRIAL DIVERSITY Clinical trial diversity helps to ensure we have medications that are suited to reflect and treat the intended treatment population. That’s why our entire industry came together to develop and voluntarily adopt principles on closing the diversity gaps. Understanding the challenges of PHRMA STATEMENT ON HOUSE LEADERSHIP’S “PARTISAN” DRUG PhRMA Statement on House Leadership’s “Partisan” Drug Pricing Proposal. WASHINGTON, D.C. (April 22, 2021) – Pharmaceutical Research and Manufacturers of America president and CEO Stephen J. Ubl issued the following statement today after House Democratic leaders released their partisan drug pricing proposal: “The American peoplewant
FOLLOW THE DOLLAR REPORT Follow the Dollar Report. This paper provides a high-level explanation of the financial flows that occur as brand medicines move through the supply chain for retail, mail-order and specialty drugs. Download the Executive Summary. Download the Report. -. BIOPHARMACEUTICAL DIGITAL HEALTH LEXICON Digital health is transforming nearly every aspect of our health care system, improving efficiency, expanding access to treatments and technologies, and ushering in increased development of personalized medicine. One of the foundational elements of a modern digital R&D regulatory framework is a common lexicon and understanding of key terms to orient stakeholders and facilitate CODE ON INTERACTIONS Therefore, PhRMA adopts this updated and enhanced voluntary Code on relationships with U.S. health care professionals. This Code reflects and builds upon the standards and principles set forth in BIOPHARMACEUTICAL RESEARCH & DEVELOPMENT phase i phase ii phase iii phase iv ind submitted tens number of volunteers hundreds thousands nda/bla submitted fda approval the biopharmaceutical research and development process INNOVATIVE CONTRACTING: OPPORTUNITIES AND CHALLENGES INNOVATIVE CONTRACTS CAN BE BENEFICIAL TO PATIENTS AND LOWER OUT-OF-POCKET COSTS WHILE PROVIDING SAVINGS FOR THE HEALTH SYSTEM. 1 Avalere. More than Half of Health Plans Use Outcomes-Based Contracts.CODES & GUIDELINES
Codes & Guidelines. PhRMA represents the nation’s leading biopharmaceutical research companies. Our success in developing and delivering medicines to help patients live longer and healthier lives depends on ethical relationships and behavior. Browse key Codes and PHRMA’S EQUITY INITIATIVE PhRMA CAREs Grant: Addressing Racial Disparities in Medication Utilization and Adherence. In 2019, PhRMA established the Health Equity Roundtable with the goal of improving health outcomes by addressing inequities in care. As part of the Health Equity Roundtable, PhRMA is offering funding opportunities to spur ideas for practical interventions MEDICINES IN DEVELOPMENT Medicines in Development for Antimicrobial Resistance 2021 Report. Today, more than 1,300 medicines and vaccines for various cancers are currently in development by innovative biopharmaceutical research companies, all of which are in clinical trials or awaiting review by CLINICAL TRIAL DIVERSITY Clinical trial diversity helps to ensure we have medications that are suited to reflect and treat the intended treatment population. That’s why our entire industry came together to develop and voluntarily adopt principles on closing the diversity gaps. Understanding the challenges of PHRMA STATEMENT ON HOUSE LEADERSHIP’S “PARTISAN” DRUG PhRMA Statement on House Leadership’s “Partisan” Drug Pricing Proposal. WASHINGTON, D.C. (April 22, 2021) – Pharmaceutical Research and Manufacturers of America president and CEO Stephen J. Ubl issued the following statement today after House Democratic leaders released their partisan drug pricing proposal: “The American peoplewant
FOLLOW THE DOLLAR REPORT Follow the Dollar Report. This paper provides a high-level explanation of the financial flows that occur as brand medicines move through the supply chain for retail, mail-order and specialty drugs. Download the Executive Summary. Download the Report. -. BIOPHARMACEUTICAL DIGITAL HEALTH LEXICON Digital health is transforming nearly every aspect of our health care system, improving efficiency, expanding access to treatments and technologies, and ushering in increased development of personalized medicine. One of the foundational elements of a modern digital R&D regulatory framework is a common lexicon and understanding of key terms to orient stakeholders and facilitate CODE ON INTERACTIONS Therefore, PhRMA adopts this updated and enhanced voluntary Code on relationships with U.S. health care professionals. This Code reflects and builds upon the standards and principles set forth in BIOPHARMACEUTICAL RESEARCH & DEVELOPMENT phase i phase ii phase iii phase iv ind submitted tens number of volunteers hundreds thousands nda/bla submitted fda approval the biopharmaceutical research and development process INNOVATIVE CONTRACTING: OPPORTUNITIES AND CHALLENGES INNOVATIVE CONTRACTS CAN BE BENEFICIAL TO PATIENTS AND LOWER OUT-OF-POCKET COSTS WHILE PROVIDING SAVINGS FOR THE HEALTH SYSTEM. 1 Avalere. More than Half of Health Plans Use Outcomes-Based Contracts.PHRMA ORG | PHRMA
Working Together to Fight COVID-19. The Pharmaceutical Research and Manufacturers of America, PhRMA, represents the country’s leading biopharmaceutical researchers MEDICINES IN DEVELOPMENT Medicines in Development for Antimicrobial Resistance 2021 Report. Today, more than 1,300 medicines and vaccines for various cancers are currently in development by innovative biopharmaceutical research companies, all of which are in clinical trials or awaiting review by GET HELP WITH YOUR PRESCRIPTIONS Navigating the complexities of today’s health care system can be confusing and overwhelming, but it doesn’t have to be. America’s biopharmaceutical research companies that make up PhRMA have partnered with health care providers, pharmacists, patient advocacy organizations and community groups to help patients afford their medicines by creating the Medicine Assistance Tool (MAT). PHRMA STATEMENT ON HOUSE LEADERSHIP’S “PARTISAN” DRUG WASHINGTON, D.C. (April 22, 2021) – Pharmaceutical Research and Manufacturers of America president and CEO Stephen J. Ubl issued the following statement today after House Democratic leaders released their partisan drug pricing proposal: “The American people want to end the pandemic, get the economy back on track and make health care more affordable and predictable.ACCESS TO MEDICINES
Patient access to the medicines they need is critical both for individuals and for our health care system more broadly. In the United States, patients can access medicines a number of ways, including through employer-sponsored health plan, a health insurance exchange plan or a program like Medicare or Medicaid. Today, Americans havefaster
COMING TOGETHER TO FIGHT COVID-19: A CONVERSATION WITH Stephen J. Ubl Stephen J. Ubl is president and chief executive officer of PhRMA. Mr. Ubl leads PhRMA’s work preserving and strengthening a health care and economic environment that encourages medical innovation, new drug discovery and access to life-saving medicines. PRINCIPLES ON CONDUCT OF CLINICAL TRIALS PhRMA Principles on Conduct of Clinical Trials. Developing new therapies to treat disease and to improve quality of life is a long and complex process. A critical part of that process is clinical research, the study of a pharmaceutical product in humans. Without clinical research studies, no new medicines could be made available topatients.
INFOGRAPHICS ON OBTAINING PATENTS AND MAINTAINING PATENTS Intellectual property (IP) protections, including patents, are the foundation for biopharmaceutical innovation and the development of new treatments, cures and vaccines for patients. The U.S. patent system provides critical incentives for innovation and fuels the creation of new medicines. Yet, there can be confusion around what it takes for a patent to be granted and maintained. These two HOW RESEARCH EVOLVES AND BRINGS NEW HOPE TO PATIENTS Stephen J. Ubl Stephen J. Ubl is president and chief executive officer of PhRMA. Mr. Ubl leads PhRMA’s work preserving and strengthening a health care and economic environment that encourages medical innovation, new drug discovery and access to life-saving medicines. CONTINUED R&D INTO ALZHEIMER’S DISEASE MEANS HOPE FOR More than 6 million Americans, most of them age 65 or older, live with Alzheimer’s disease, a devastating degenerative brain disease and the most common form of dementia. Despite the immense challenges to research, biopharmaceutical companies remain committed. PHRMA ORG | PHRMAMEMBERS SITEEVENTSSTAY CONNECTEDBLOGDRUG DISCOVERYHOMEPAGE HEADER BAR Working Together to Fight COVID-19. The Pharmaceutical Research and Manufacturers of America, PhRMA, represents the country’s leading biopharmaceutical researchers and biotechnology companies.CODES & GUIDELINES
Codes & Guidelines. PhRMA represents the nation’s leading biopharmaceutical research companies. Our success in developing and delivering medicines to help patients live longer and healthier lives depends on ethical relationships and behavior. Browse key Codes and GET HELP WITH YOUR PRESCRIPTIONS Navigating the complexities of today’s health care system can be confusing and overwhelming, but it doesn’t have to be. America’s biopharmaceutical research companies that make up PhRMA have partnered with health care providers, pharmacists, patient advocacy organizations and community groups to help patients afford their medicines by creating the Medicine Assistance Tool (MAT). BIOPHARMACEUTICAL DIGITAL HEALTH LEXICON Digital health is transforming nearly every aspect of our health care system, improving efficiency, expanding access to treatments and technologies, and ushering in increased development of personalized medicine. One of the foundational elements of a modern digital R&D regulatory framework is a common lexicon and understanding of key terms to orient stakeholders and facilitate CODE ON INTERACTIONS WITH HEALTH CARE PROFESSIONALS This Code reflects and builds upon the standards and principles set forth in its predecessor, the PhRMA Code on Interactions with Health Care Professionals that took effect in January 2009. Like the 2009 edition, this Code addresses interactions with respect to marketed products and related pre-launch activities.STEPHEN J UBL
Stephen J. Ubl is president and chief executive officer of the Pharmaceutical Research and Manufacturers of America (PhRMA), which represents America’s leading biopharmaceutical research companies.The U.S. biopharmaceutical sector directly employs more than 800,000 Americans and invests more than $100 billion in research and development annually -- more than any other industry in CODE ON INTERACTIONS Therefore, PhRMA adopts this updated and enhanced voluntary Code on relationships with U.S. health care professionals. This Code reflects and builds upon the standards and principles set forth in STATEMENT ON APPLICATION OF PHRMA CODE SECTION 2 DURING 1 Statement on Application of PhRMA Code Section 2 During Emergency Periods June 30, 2020 Biopharmaceutical company representatives play an important role in delivering accurate, up-to-RICHARD MOSCICKI MD
Richard (Rich) A. Moscicki (Mo-shis-ke), M.D., is the executive vice president of science and regulatory advocacy and the chief medical officer at the Pharmaceutical Research and Manufacturers of America (PhRMA). Dr. Moscicki came to PhRMA in 2017 after serving as the deputy center director for science operations for the U.S. Food andDrug
PREA AND BPCA
PREA AND BPCA: SPURRING PEDIATRIC DRUG DEVELOPMENT HISTORIC CHALLENGE: Prior to 1997, which is when the first pediatric drug development incentive legislation was enacted as part PHRMA ORG | PHRMAMEMBERS SITEEVENTSSTAY CONNECTEDBLOGDRUG DISCOVERYHOMEPAGE HEADER BAR Working Together to Fight COVID-19. The Pharmaceutical Research and Manufacturers of America, PhRMA, represents the country’s leading biopharmaceutical researchers and biotechnology companies.CODES & GUIDELINES
Codes & Guidelines. PhRMA represents the nation’s leading biopharmaceutical research companies. Our success in developing and delivering medicines to help patients live longer and healthier lives depends on ethical relationships and behavior. Browse key Codes and GET HELP WITH YOUR PRESCRIPTIONS Navigating the complexities of today’s health care system can be confusing and overwhelming, but it doesn’t have to be. America’s biopharmaceutical research companies that make up PhRMA have partnered with health care providers, pharmacists, patient advocacy organizations and community groups to help patients afford their medicines by creating the Medicine Assistance Tool (MAT). BIOPHARMACEUTICAL DIGITAL HEALTH LEXICON Digital health is transforming nearly every aspect of our health care system, improving efficiency, expanding access to treatments and technologies, and ushering in increased development of personalized medicine. One of the foundational elements of a modern digital R&D regulatory framework is a common lexicon and understanding of key terms to orient stakeholders and facilitate CODE ON INTERACTIONS WITH HEALTH CARE PROFESSIONALS This Code reflects and builds upon the standards and principles set forth in its predecessor, the PhRMA Code on Interactions with Health Care Professionals that took effect in January 2009. Like the 2009 edition, this Code addresses interactions with respect to marketed products and related pre-launch activities.STEPHEN J UBL
Stephen J. Ubl is president and chief executive officer of the Pharmaceutical Research and Manufacturers of America (PhRMA), which represents America’s leading biopharmaceutical research companies.The U.S. biopharmaceutical sector directly employs more than 800,000 Americans and invests more than $100 billion in research and development annually -- more than any other industry in CODE ON INTERACTIONS Therefore, PhRMA adopts this updated and enhanced voluntary Code on relationships with U.S. health care professionals. This Code reflects and builds upon the standards and principles set forth in STATEMENT ON APPLICATION OF PHRMA CODE SECTION 2 DURING 1 Statement on Application of PhRMA Code Section 2 During Emergency Periods June 30, 2020 Biopharmaceutical company representatives play an important role in delivering accurate, up-to-RICHARD MOSCICKI MD
Richard (Rich) A. Moscicki (Mo-shis-ke), M.D., is the executive vice president of science and regulatory advocacy and the chief medical officer at the Pharmaceutical Research and Manufacturers of America (PhRMA). Dr. Moscicki came to PhRMA in 2017 after serving as the deputy center director for science operations for the U.S. Food andDrug
PREA AND BPCA
PREA AND BPCA: SPURRING PEDIATRIC DRUG DEVELOPMENT HISTORIC CHALLENGE: Prior to 1997, which is when the first pediatric drug development incentive legislation was enacted as partABOUT | PHRMA
About. The Pharmaceutical Research and Manufacturers of America (PhRMA) represents the country’s leading innovative biopharmaceutical research companies, which are devoted to discovering and developing medicines that enable patients to live longer, healthier and more productive lives. Since 2000, PhRMA member companies have invested nearly $1 PHRMA’S EQUITY INITIATIVE PhRMA CAREs Grant: Addressing Racial Disparities in Medication Utilization and Adherence. In 2019, PhRMA established the Health Equity Roundtable with the goal of improving health outcomes by addressing inequities in care. As part of the Health Equity Roundtable, PhRMA is offering funding opportunities to spur ideas for practical interventionsIN THE PIPELINE
With more than 8,000 medicines in development, 74% of which are potentially first-in-class, patients have more reasons to be optimistic than ever before. Medicines and vaccines are being developed across dozens of therapeutic areas – including COVID-19, cancer, diabetes, cardiovascular, Alzheimer’s disease and MEDICINES IN DEVELOPMENT Medicines in Development for Antimicrobial Resistance 2021 Report. Today, more than 1,300 medicines and vaccines for various cancers are currently in development by innovative biopharmaceutical research companies, all of which are in clinical trials or awaiting review by BIOPHARMACEUTICAL DIGITAL HEALTH LEXICON Digital health is transforming nearly every aspect of our health care system, improving efficiency, expanding access to treatments and technologies, and ushering in increased development of personalized medicine. One of the foundational elements of a modern digital R&D regulatory framework is a common lexicon and understanding of key terms to orient stakeholders and facilitate REPORT: INDUSTRY PROFILE 2019 Industry Profile 2019. To download the full report, click here. The Profile is PhRMA’s flagship publication for telling the story of the sector for nearly five decades. It outlines what the industry stands for—including key policy solutions—along with an advocacy toolkiton key issue areas.
CLINICAL TRIAL DIVERSITY Clinical trial diversity helps to ensure we have medications that are suited to reflect and treat the intended treatment population. That’s why our entire industry came together to develop and voluntarily adopt principles on closing the diversity gaps. Understanding the challenges of DIRECT TO CONSUMER ADVERTISING PRINCIPLES Direct to Consumer Advertising Principles. In October 2018, PhRMA’s Board of Directors adopted measures to enhance the PhRMA Guiding Principles on Direct to Consumer Advertisements about Prescription Medicines. The revised, voluntary Principles become effective on April 15, 2019 and include a new guiding principle stating that “ llDTC
RESEARCHING ALZHEIMER’S MEDICINES Society’s Great Challenge More than 6 million Americans impacted 6th leading cause of death in the U.S. $355 billion each year in direct medical costs More than 11 million caregivers providing $257 billion in uncompensated care Black Americans are twice as likely and Latinos are 1.5 times more likely to develop Alzheimer’s than non-Hispanicwhite Americans
JAMES C STANSEL
James C. Stansel is executive vice president, general counsel and corporate secretary of the Pharmaceutical Research and Manufacturers of America (PhRMA), where he is responsible for leading a team of lawyers in supporting PhRMA’s policy, advocacy and science priorities and in the development of sound legal policies impacting the pharmaceutical industry. PHRMA ORG | PHRMAMEMBERS SITEEVENTSSTAY CONNECTEDBLOGDRUG DISCOVERYHOMEPAGE HEADER BAR Working Together to Fight COVID-19. The Pharmaceutical Research and Manufacturers of America, PhRMA, represents the country’s leading biopharmaceutical researchers and biotechnology companies.CODES & GUIDELINES
Codes & Guidelines. PhRMA represents the nation’s leading biopharmaceutical research companies. Our success in developing and delivering medicines to help patients live longer and healthier lives depends on ethical relationships and behavior. Browse key Codes and GET HELP WITH YOUR PRESCRIPTIONS Navigating the complexities of today’s health care system can be confusing and overwhelming, but it doesn’t have to be. America’s biopharmaceutical research companies that make up PhRMA have partnered with health care providers, pharmacists, patient advocacy organizations and community groups to help patients afford their medicines by creating the Medicine Assistance Tool (MAT). BIOPHARMACEUTICAL DIGITAL HEALTH LEXICON Digital health is transforming nearly every aspect of our health care system, improving efficiency, expanding access to treatments and technologies, and ushering in increased development of personalized medicine. One of the foundational elements of a modern digital R&D regulatory framework is a common lexicon and understanding of key terms to orient stakeholders and facilitate CODE ON INTERACTIONS WITH HEALTH CARE PROFESSIONALS This Code reflects and builds upon the standards and principles set forth in its predecessor, the PhRMA Code on Interactions with Health Care Professionals that took effect in January 2009. Like the 2009 edition, this Code addresses interactions with respect to marketed products and related pre-launch activities.STEPHEN J UBL
Stephen J. Ubl is president and chief executive officer of the Pharmaceutical Research and Manufacturers of America (PhRMA), which represents America’s leading biopharmaceutical research companies.The U.S. biopharmaceutical sector directly employs more than 800,000 Americans and invests more than $100 billion in research and development annually -- more than any other industry in CODE ON INTERACTIONS Therefore, PhRMA adopts this updated and enhanced voluntary Code on relationships with U.S. health care professionals. This Code reflects and builds upon the standards and principles set forth in STATEMENT ON APPLICATION OF PHRMA CODE SECTION 2 DURING 1 Statement on Application of PhRMA Code Section 2 During Emergency Periods June 30, 2020 Biopharmaceutical company representatives play an important role in delivering accurate, up-to-RICHARD MOSCICKI MD
Richard (Rich) A. Moscicki (Mo-shis-ke), M.D., is the executive vice president of science and regulatory advocacy and the chief medical officer at the Pharmaceutical Research and Manufacturers of America (PhRMA). Dr. Moscicki came to PhRMA in 2017 after serving as the deputy center director for science operations for the U.S. Food andDrug
PREA AND BPCA
PREA AND BPCA: SPURRING PEDIATRIC DRUG DEVELOPMENT HISTORIC CHALLENGE: Prior to 1997, which is when the first pediatric drug development incentive legislation was enacted as part PHRMA ORG | PHRMAMEMBERS SITEEVENTSSTAY CONNECTEDBLOGDRUG DISCOVERYHOMEPAGE HEADER BAR Working Together to Fight COVID-19. The Pharmaceutical Research and Manufacturers of America, PhRMA, represents the country’s leading biopharmaceutical researchers and biotechnology companies.CODES & GUIDELINES
Codes & Guidelines. PhRMA represents the nation’s leading biopharmaceutical research companies. Our success in developing and delivering medicines to help patients live longer and healthier lives depends on ethical relationships and behavior. Browse key Codes and GET HELP WITH YOUR PRESCRIPTIONS Navigating the complexities of today’s health care system can be confusing and overwhelming, but it doesn’t have to be. America’s biopharmaceutical research companies that make up PhRMA have partnered with health care providers, pharmacists, patient advocacy organizations and community groups to help patients afford their medicines by creating the Medicine Assistance Tool (MAT). BIOPHARMACEUTICAL DIGITAL HEALTH LEXICON Digital health is transforming nearly every aspect of our health care system, improving efficiency, expanding access to treatments and technologies, and ushering in increased development of personalized medicine. One of the foundational elements of a modern digital R&D regulatory framework is a common lexicon and understanding of key terms to orient stakeholders and facilitate CODE ON INTERACTIONS WITH HEALTH CARE PROFESSIONALS This Code reflects and builds upon the standards and principles set forth in its predecessor, the PhRMA Code on Interactions with Health Care Professionals that took effect in January 2009. Like the 2009 edition, this Code addresses interactions with respect to marketed products and related pre-launch activities.STEPHEN J UBL
Stephen J. Ubl is president and chief executive officer of the Pharmaceutical Research and Manufacturers of America (PhRMA), which represents America’s leading biopharmaceutical research companies.The U.S. biopharmaceutical sector directly employs more than 800,000 Americans and invests more than $100 billion in research and development annually -- more than any other industry in CODE ON INTERACTIONS Therefore, PhRMA adopts this updated and enhanced voluntary Code on relationships with U.S. health care professionals. This Code reflects and builds upon the standards and principles set forth in STATEMENT ON APPLICATION OF PHRMA CODE SECTION 2 DURING 1 Statement on Application of PhRMA Code Section 2 During Emergency Periods June 30, 2020 Biopharmaceutical company representatives play an important role in delivering accurate, up-to-RICHARD MOSCICKI MD
Richard (Rich) A. Moscicki (Mo-shis-ke), M.D., is the executive vice president of science and regulatory advocacy and the chief medical officer at the Pharmaceutical Research and Manufacturers of America (PhRMA). Dr. Moscicki came to PhRMA in 2017 after serving as the deputy center director for science operations for the U.S. Food andDrug
PREA AND BPCA
PREA AND BPCA: SPURRING PEDIATRIC DRUG DEVELOPMENT HISTORIC CHALLENGE: Prior to 1997, which is when the first pediatric drug development incentive legislation was enacted as partABOUT | PHRMA
About. The Pharmaceutical Research and Manufacturers of America (PhRMA) represents the country’s leading innovative biopharmaceutical research companies, which are devoted to discovering and developing medicines that enable patients to live longer, healthier and more productive lives. Since 2000, PhRMA member companies have invested nearly $1 PHRMA’S EQUITY INITIATIVE PhRMA CAREs Grant: Addressing Racial Disparities in Medication Utilization and Adherence. In 2019, PhRMA established the Health Equity Roundtable with the goal of improving health outcomes by addressing inequities in care. As part of the Health Equity Roundtable, PhRMA is offering funding opportunities to spur ideas for practical interventionsIN THE PIPELINE
With more than 8,000 medicines in development, 74% of which are potentially first-in-class, patients have more reasons to be optimistic than ever before. Medicines and vaccines are being developed across dozens of therapeutic areas – including COVID-19, cancer, diabetes, cardiovascular, Alzheimer’s disease and MEDICINES IN DEVELOPMENT Medicines in Development for Antimicrobial Resistance 2021 Report. Today, more than 1,300 medicines and vaccines for various cancers are currently in development by innovative biopharmaceutical research companies, all of which are in clinical trials or awaiting review by BIOPHARMACEUTICAL DIGITAL HEALTH LEXICON Digital health is transforming nearly every aspect of our health care system, improving efficiency, expanding access to treatments and technologies, and ushering in increased development of personalized medicine. One of the foundational elements of a modern digital R&D regulatory framework is a common lexicon and understanding of key terms to orient stakeholders and facilitate REPORT: INDUSTRY PROFILE 2019 Industry Profile 2019. To download the full report, click here. The Profile is PhRMA’s flagship publication for telling the story of the sector for nearly five decades. It outlines what the industry stands for—including key policy solutions—along with an advocacy toolkiton key issue areas.
CLINICAL TRIAL DIVERSITY Clinical trial diversity helps to ensure we have medications that are suited to reflect and treat the intended treatment population. That’s why our entire industry came together to develop and voluntarily adopt principles on closing the diversity gaps. Understanding the challenges of DIRECT TO CONSUMER ADVERTISING PRINCIPLES Direct to Consumer Advertising Principles. In October 2018, PhRMA’s Board of Directors adopted measures to enhance the PhRMA Guiding Principles on Direct to Consumer Advertisements about Prescription Medicines. The revised, voluntary Principles become effective on April 15, 2019 and include a new guiding principle stating that “ llDTC
RESEARCHING ALZHEIMER’S MEDICINES Society’s Great Challenge More than 6 million Americans impacted 6th leading cause of death in the U.S. $355 billion each year in direct medical costs More than 11 million caregivers providing $257 billion in uncompensated care Black Americans are twice as likely and Latinos are 1.5 times more likely to develop Alzheimer’s than non-Hispanicwhite Americans
JAMES C STANSEL
James C. Stansel is executive vice president, general counsel and corporate secretary of the Pharmaceutical Research and Manufacturers of America (PhRMA), where he is responsible for leading a team of lawyers in supporting PhRMA’s policy, advocacy and science priorities and in the development of sound legal policies impacting the pharmaceutical industry. Skip to main content PhRMA LogoPhRMA logo with words Research, Progress, and Hopeunderneath
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PhRMA represents the country’s leading biopharmaceutical research companies and supports the search for new treatments and cures. PhRMA’s Equity Initiative Industry Profile 2020* Advocacy
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Learn more about America's biopharmaceutical companies and how they seek to improve patients' lives. A search engine designed to find resources available through the various biopharmaceutical industry programs.__Learn More
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A search engine designed to find resources available through the various biopharmaceutical industry programs. Many Americans are struggling to afford their medicines and have important questions about their medicine costs. Let's Talk About Cost addresses these questions.__Learn More
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Many Americans are struggling to afford their medicines and have important questions about their medicine costs. Let's Talk About Cost addresses these questions. There are right and wrong prescriptions for changing Medicare. Seniors need Washington to focus on the right ones.__Learn More
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There are right and wrong prescriptions for changing Medicare. Seniors need Washington to focus on the right ones. The PhRMA Foundation supports the research and career endeavors of scientists in drug discovery and development.__Learn More
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The PhRMA Foundation supports the research and career endeavors of scientists in drug discovery and development. We Work For Health aims to increase awareness by uniting workers throughout the industry.__Learn More
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are in clinical testingLearn More
550
NEW MEDICINES
Approved by the Food and Drug Administration since 2000.Learn More
$2.6
BILLION
The average cost to develop one new medicine.8
MONTHS
Priority FDA review time thanks to PDUFA74%
OF MEDICINES IN DEVELOPMENT have the potential to be first in class medicinesLearn More
160+
MEDICINES IN DEVELOPMENT for diabetes and related conditionsLearn More
80+
AUTOIMMUNE DISEASES
have been identified to-date$3.5
MILLION
Average yearly amount PhRMA Foundation awards to young scientistsLearn More
7,000
NEW MEDICINES
Currently in development around the world.90%
OF ALL CLINICAL TRIALS are led by the biopharmaceutical industryLearn More
$1.1
TRILLION
total value of goods and services supported by the biopharmaceuticalsector
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4,500
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4.7
MILLION JOBS
are supported by America's biopharmaceutical companiesLearn More
45%
of all Medicare acute hospitals participate in 340B.Learn More
30,000
340B sites enrolled as of May 2015.Learn More
88%
DECLINE IN HIV/AIDS DEATH RATESSince the 1990s
80%
of 340B volume goes through DSH hospitals even though they make up just 9% of 340B entities.Learn More
1,500
NEW SAFE AND EFFECTIVE MEDICATIONS have been delivered to patients, thanks to PDUFA.Learn More
1,300+
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are in clinical testingLearn More
550
NEW MEDICINES
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$2.6
BILLION
The average cost to develop one new medicine.8
MONTHS
Priority FDA review time thanks to PDUFA74%
OF MEDICINES IN DEVELOPMENT have the potential to be first in class medicinesLearn More
160+
MEDICINES IN DEVELOPMENT for diabetes and related conditionsLearn More
80+
AUTOIMMUNE DISEASES
have been identified to-date$3.5
MILLION
Average yearly amount PhRMA Foundation awards to young scientistsLearn More
7,000
NEW MEDICINES
Currently in development around the world.90%
OF ALL CLINICAL TRIALS are led by the biopharmaceutical industryLearn More
$1.1
TRILLION
total value of goods and services supported by the biopharmaceuticalsector
Learn More
4,500
INDUSTRY SPONSORED CLINICAL TRIALS are currently underwayLearn More
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MILLION JOBS
are supported by America's biopharmaceutical companiesLearn More
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of all Medicare acute hospitals participate in 340B.Learn More
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340B sites enrolled as of May 2015.Learn More
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DECLINE IN HIV/AIDS DEATH RATESSince the 1990s
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of 340B volume goes through DSH hospitals even though they make up just 9% of 340B entities.Learn More
1,500
NEW SAFE AND EFFECTIVE MEDICATIONS have been delivered to patients, thanks to PDUFA.Learn More
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