Brittany Dustman
Director, Global Regulatory Affairs - Cell Therapy at Bristol Myers Squibb | Greater Philadelphia
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Brittany Dustman serves as the Director of Global Regulatory Affairs for Cell Therapy at Bristol Myers Squibb, where she leverages her extensive expertise in regulatory affairs to drive the development and commercialization of innovative therapies. With a robust background in oncology, immunology, and respiratory therapeutic areas, Brittany is adept at navigating the complexities of regulatory landscapes for small molecules, biologics, and advanced therapies like cell and gene therapies.
In her current role, Brittany is pivotal in shaping the U.S. regulatory strategy for a marketed cell therapy, focusing on expanding its indications through a supplemental Biologics License Application (sBLA). She is responsible for coordinating the preparations for this major application, which includes strategizing for a pre-sBLA meeting with the FDA. Brittany collaborates closely with cross-functional teams, ensuring that the objectives, content, and overall strategy align with regulatory requirements and market needs. Her ability to integrate insights from clinical trials and pharmacoeconomics into regulatory submissions enhances the likelihood of successful outcomes, ultimately benefiting patients in need of cutting-edge therapies.
Brittany’s skills in medication therapy management, clinical pharmacy, and pharmacology further enrich her contributions, allowing her to effectively communicate complex scientific data to regulatory authorities while advocating for patient access to life-changing treatments. Her commitment to excellence in regulatory affairs not only supports Bristol Myers Squibb’s mission to deliver transformative therapies but also positions her as a thought leader in the evolving landscape of cell therapy regulation.
Director, Global Regulatory Affairs - Cell Therapy at Bristol Myers Squibb in February 2022 to Present
Pharmacist at CVS Health in May 2011 to April 2022
Associate Director, Global Regulatory Affairs - Oncology, Cell and Gene Therapy at GSK in May 2020 to February 2022
Manager Global Regulatory Affairs at GSK in June 2018 to April 2020
Postdoctoral Global Regulatory Affairs Fellow at GSK in July 2016 to May 2018
Student Extern, Divisions of Neurology and Psychiatry, CDER at FDA in January 2016 to February 2016
New Product Research Intern, Respiratory Health at GSK in May 2014 to August 2014
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Temple University School of Pharmacy, Doctor of Pharmacy (PharmD), January 2012 to January 2016
Temple University School of Pharmacy Graduate Program, Master’s Degree, January 2015 to January 2016
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Pharmacy
Pharmaceutical Industry
Pharmacists
Clinical Trials
Patient Counseling
Clinical Pharmacology
Pharmacy Practice
Medicare Part D
Hospital Pharmacy
Pharmacoeconomics
Prescription
Managed Care
Leadership
Customer Service
Drug Development
Medication Therapy Management
Compounding
Pharmacy Benefit Management
Community Pharmacy
Clinical Pharmacy
Pharmacology
Pharmacueticals
Diabetes
Pharmacokinetics
Marketing
Communication
Strategic Planning
Regulatory Affairs
Pharmacovigilance
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Discover more about Bristol Myers SquibbWhat is Brittany Dustman email address?
Email Brittany Dustman at [email protected]. This email is the most updated Brittany Dustman's email found in 2026.
How to contact Brittany Dustman?
To contact Brittany Dustman send an email to [email protected].
What company does Brittany Dustman work for?
Brittany Dustman works for Bristol Myers Squibb
What is Brittany Dustman's role at Bristol Myers Squibb?
Brittany Dustman is Director, Global Regulatory Affairs - Cell Therapy
What is Brittany Dustman's Phone Number?
Brittany Dustman's phone (**) *** *** 206
What industry does Brittany Dustman work in?
Brittany Dustman works in the Pharmaceuticals industry.
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