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The U.S Food and Drug Administration (FDA) plays a critical role in protecting and promoting the health of all Americans. Every day, the FDA does important work to ensure the safety, efficacy and security of our nation’s medical products, including human drugs and biologics. From reviewing the drug profile of a first-in-class medicine up for approval, to inspecting a medicine’s manufacturing site, the FDA’s experts engage in a range of regulatory review activities intended to bring safe and effective new medicines to patients in a timely manner. In the past year alone, the FDA approved a record number of new medicines to fight a range of diseases, including multiple sclerosis, Alzheimer’s disease and Parkinson’s disease. 

The FDA is also on the front lines helping to deliver increased personalized medicine access to patients. The agency’s efforts approving new immunotherapy and cell and gene-based therapy treatment options, which harness a patient’s own immune system to defeat a disease, are revolutionizing the treatment paradigm. At the same time, the agency is enhancing a competitive biopharmaceutical marketplace, including approving a record-setting number of generic medicines in 2017.

None of these milestones would have been possible without the dedicated professionals who work at FDA and contribute to the agency being recognized as the gold-standard for the regulatory review of drugs and biologics. I should know: during my time at the FDA as the Deputy Center Director for Science Operations for the Center for Drug Evaluation and Research, I had the privilege of working with these talented professionals who bring to bear their expertise and hard work to fulfill the FDA’s public health oversight mission and ensure the medicines we take are safe and effective for ourselves and our loved ones.

A stable and sustainable workforce is crucial to the FDA’s success in keeping pace with scientific advances in biopharmaceutical drug development and ensuring safe and effective innovative medicines reach patients in a timely manner. However, the FDA has faced significant human resource challenges in recent years, requiring that the agency and the biopharmaceutical industry work together to find solutions to enhance its recruiting and hiring.

Under the sixth authorization of the Prescription Drug User Fee Act (PDUFA VI), the second authorization of the Biosimilar User Fee Act (BsUFA II), and through passage of the 21st Century Cures Act, the FDA has been given additional resources and new hiring and pay authorities to build and maintain the agency’s workforce. These include agency hiring goals and related recruitment and retention initiatives, a hiring pilot intended to modernize and streamline hiring processes, and establishment of a dedicated staffing team charged with the continuous recruiting, staffing, and retention of scientific, technical and professional staff – the biostatisticians, medical reviewers, and project managers, just to name a few - who want to make a difference in the lives of Americans.

America’s biopharmaceutical companies are taking bold steps to develop medicines to treat life-threatening diseases and give hope to patients, providers and caregivers alike, as well as bring value to the health care system. But we can’t do it alone. As we embark on this new era of medicine, the FDA must continue to grow its team of dedicated professionals ready to tackle some of the most complex medical issues of our time. If you are interested in serving, please visit the agency’s hiring page.

Richard Moscicki M D

Dr. Moscicki served as executive vice president, Science and Regulatory Advocacy and chief medical officer at PhRMA from 2017-summer of 2022. He joined the organization after serving as the Deputy Center Director for Science Operations for the U.S. Food and Drug Administration’s (FDA) Center for Drug Evaluation and Research (CDER) since 2013. While at FDA, Dr. Moscicki brought executive direction of Center operations and leadership in overseeing the development, implementation, and direction of CDER’s programs. Previous positions include serving as Chief Medical Officer at Genzyme Corporation from 1992 to 2011, where he was responsible for worldwide global regulatory and pharmacovigilance matters, as well as all aspects of clinical research and medical affairs for the company. He served as the senior vice president and head of Clinical Development at Sanofi-Genzyme from 2011-2013.

Richard Moscicki M D

Why PDUFA VIII keeps patients first and strengthens America's biopharma leadership

September 15, 2026

Mass compounding puts patients at risk

July 16, 2026

PDUFA creates an efficient drug review process that benefits American patients

April 22, 2026

Advancing patient care: A look at new medicines approved in 2025

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Knockoffs of FDA-approved drugs put patients at risk

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PDUFA: Essential to America’s edge in drug development and patient access

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Major drug compounder is spending millions on misleading Super Bowl ad

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Preventing and fighting disease: A look at the biopharmaceutical progress made for patients in 2024

February 3, 2025

More oversight needed of unapproved medicines that threaten patients’ health

August 1, 2024

The use of real-world data in drug development

May 13, 2024

New analysis: Accelerated approval pathway is changing lives in underserved communities

April 30, 2024

Novel treatments and vaccines approved for U.S. patients in 2023 reach five-year high

January 23, 2024

Florida’s importation plan puts patients in danger

January 5, 2024

The Biopharmaceutical Industry Still Needs Clarity from the FDA on Orange Book Listings

December 19, 2023

Decentralized clinical trials and the future of drug development

August 9, 2023

How FDA’s modernization strategy could improve drug development

June 20, 2023

Setting the record straight on accelerated approval

May 22, 2023

FDA should remain the authority on the safety and effectiveness of medicines

April 12, 2023

Novel medicines approved in 2022 offer increased treatment options for patients

January 23, 2023

What you should know about real-world evidence and drug development

December 19, 2022

Three things to know about the accelerated approval pathway

December 12, 2022

PDUFA and BsUFA reauthorizations are wins for patients

October 5, 2022

Timely reauthorization of PDUFA and BsUFA is vital to the FDA’s review of medicines

September 12, 2022

Word of the Month: Biomarkers and surrogate endpoints

July 11, 2022

Ensuring timely reauthorization of PDUFA and BsUFA

May 11, 2022

ICYMI: New resource catalogs biopharmaceutical industry lessons learned from COVID-19

April 28, 2022

The accelerated approval pathway: Helping patients with serious or life-threatening diseases

March 17, 2022

The importance of timely PDUFA and BsUFA reauthorization

February 3, 2022

ICYMI: New approvals by the FDA in 2021 offer greater treatment options for patients

January 26, 2022

World AIDS Day: Remembering those we’ve lost and exploring the continued fight against HIV/AIDS

December 1, 2021

Biosimilar User Fee Act (III) Performance Goals Letter will help increase options for patients and promote competition

September 28, 2021

Meeting Tomorrow: Looking ahead to PDUFA VII

September 27, 2021

The impact of monoclonal antibodies and COVID-19 recovery

September 2, 2021

PDUFA VII is critical for future biopharmaceutical innovation and for patients

August 23, 2021

3 things that support robust biopharmaceutical research and development

June 29, 2021

How strengthening the biosimilar marketplace benefits patients

May 18, 2021

The FDA Office of Minority Health and Health Equity: Working to advance health equity through diversity in research

May 12, 2021

2020 FDA approvals show innovation despite COVID-19 pandemic challenges

January 26, 2021

Nearly 400 cell and gene therapies in development to target a broad range of diseases

March 10, 2020

ICYMI: 2019 brings innovative medicines to patients

January 17, 2020

PhRMA comments to Congress on Cures 2.0 call to action

December 18, 2019

Guest Post: Using the patient voice to go boldly

May 30, 2019

IP Explained: How Hatch-Waxman successfully balances affordability and innovation

May 22, 2019

Clinical Trials Awareness Week: Celebrating innovation in clinical research

May 15, 2019

Guest post: Hearing from patients on Rare Disease Day

February 28, 2019

Rare Disease Day: Unmet medical need inspires biopharmaceutical innovation

February 28, 2019

Why state drug importation pilot programs don’t work

February 8, 2019

Putting 2018 medicine approvals in context

January 23, 2019

Balancing innovation and competition in the biologics marketplace

October 11, 2018

New analysis shows that more medicines worldwide are available to U.S. patients

June 5, 2018

Bringing innovation to clinical trial design

April 23, 2018

Spending on medicines grew less than one percent in 2017

April 19, 2018

Rare Disease Day: Unmet need inspires innovation

February 28, 2018

Innovation comes in many forms, including new and expanded uses of existing medicines

January 29, 2018

ICYMI: Why 2017 medicine approvals matter

January 12, 2018

New surveys find payers and providers want more data from biopharmaceutical companies

December 6, 2017

Supporting opportunities for enhanced competition in the marketplace

November 22, 2017

VIDEO: PhRMA CEO discusses industry response to opioid crisis on Mornings with Maria

October 12, 2017

The next five years of PDUFA VI: Driving the availability of innovative treatments for patients

October 2, 2017

Opportunities to build upon enhanced competition for medicines in the marketplace

July 27, 2017

Why reauthorization of PDUFA matters

July 13, 2017

A critical opportunity to prevent prescription drug abuse

June 2, 2017

Guest Post: The importance of a modern FDA in drug discovery

March 22, 2017

FDA needs best and brightest to advance a new era of medicine with America’s biopharmaceutical companies

FDA

PDUFA

FDA needs best and brightest to advance a new era of medicine with America’s biopharmaceutical companies

October 16, 2018

FDA needs best and brightest to advance a new era of medicine with America’s biopharmaceutical companies

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