11/22/2021 | Press release | Distributed by Public on 11/22/2021 16:21
(WASHINGTON, Nov. 22, 2021) - The American Society of Hematology (ASH) will honor Peter Marks, MD, PhD, Director of the Center for Biologics Evaluation and Research (CBER) at the U.S. Food and Drug Administration (FDA) for his outstanding commitment to hematology in overseeing the approval of therapeutics that improve the quality of the lives of people with blood disorders. He will be recognized at the 2021 ASH Annual Meeting, December 11-14, in Atlanta, Georgia.
Dr. Marks will receive the 2021 ASH Outstanding Service Award, an honor recognizing effective leadership behind the scenes in areas relevant to the mission of the Society, and his overall commitment to advancing public health. Dr. Marks has been an active ASH member for more than 25 years, and has been instrumental in leading efforts at the FDA to respond to the COVID-19 pandemic.
"ASH is pleased to honor Dr. Marks, under whose leadership the FDA has made incredible advancements in the field of hematology, including overseeing the approvals of innovative cellular and gene-based therapies, and working to streamline the regulatory process to get innovative therapies to patients in need," said ASH President Martin S. Tallman, of Memorial Sloan Kettering Cancer Center (MSK). "Dr. Marks has a long history of engagement as a member of ASH and as a valued friend to the Society through his role at the FDA. His support and leadership have contributed to the success of joint ASH-FDA programs in recent years, as well as to the ongoing efforts to explore the use of clinically relevant real-world sickle cell disease and thalassemia data for research."
Dr. Marks, a clinician-scientist who is board certified in internal medicine and hematology and medical oncology, joined the FDA in 2012 as Deputy Center Director for CBER and became Center Director in 2016. In this role he oversees the center's work of assuring the safety and effectiveness of biological products, including vaccines, allergenic products, blood and blood products, and cellular, tissue, and gene therapies.
Dr. Marks has made hematology a key priority during his tenure at FDA. He helped the Agency lead the implementation of the 21st Century Cures Act, in which CBER rolled out the Regenerative Medicine Advanced Therapy Designation program for reviewing cell therapies and tissue-engineering products. Dr. Marks was instrumental in the success of the 2018 FDA-ASH Sickle Cell Disease Clinical Endpoints Workshop and the 2021 Real-World Evidence Stakeholder Initiative, hosted by ASH Research Collaborative (ASH RC) and Institute of Genomics Innovation (IGI), in collaboration with the FDA.
Over the past two years, his extraordinary leadership and public service during the COVID-19 pandemic and his steadfast commitment to scientific principles have bolstered public confidence in the review and approval of COVID-19 vaccines. During this tumultuous time, Dr. Marks remained a true partner to ASH, providing helpful and timely insights to the Society throughout the pandemic.
The American Society of Hematology (ASH) (www.hematology.org) is the world's largest professional society of hematologists dedicated to furthering the understanding, diagnosis, treatment, and prevention of disorders affecting the blood. For more than 60 years, the Society has led the development of hematology as a discipline by promoting research, patient care, education, training, and advocacy in hematology. ASH publishes Blood (www.bloodjournal.org), the most cited peer-reviewed publication in the field, and Blood Advances (www.bloodadvances.org), an online, peer-reviewed open-access journal.
Leah Enser, American Society of Hematology
[email protected]; 202-552-4927