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Advanced Biotherapeutics: Manufacturing and Regulatory Affairs MS
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Advanced Biotherapeutics: Manufacturing and Regulatory Affairs MS
Main Campus, Philadelphia, United States
# 301-350QS Subject Rankings
Pharmacy and PharmacologyMain Subject Area
Program overview
Main Subject
Pharmacy and Pharmacology
Degree
MSc
Study Level
Masters
Study Mode
On Campus
The Master of Science in Advanced Biotherapeutics: Manufacturing and Regulatory Affairs in the School of Pharmacy at Temple University launched in fall 2022 in collaboration with the Thomas Jefferson University’s Institute of Bioprocessing.
While global companies continue to discover new, small-molecule therapeutic agents, an important paradigm shift to large-molecule, biopharmaceutical products as well as individualized medicine (advanced biotherapeutics) has been made possible due to new advances in the biotechnology and bioprocessing communities.
Originally focused on protein replacement and monoclonal antibody based therapies, the profoundly rapid development and production of new therapeutics such as cell and gene therapies and COVID-19 vaccines based on messenger-RNA technology has further expanded the market and the need for a skilled and knowledgeable workforce.
This expansion affects every aspect of drug development, including manufacturing techniques, analytical methods and regulatory processes.
Program overview
Main Subject
Pharmacy and Pharmacology
Degree
MSc
Study Level
Masters
Study Mode
On Campus
The Master of Science in Advanced Biotherapeutics: Manufacturing and Regulatory Affairs in the School of Pharmacy at Temple University launched in fall 2022 in collaboration with the Thomas Jefferson University’s Institute of Bioprocessing.
While global companies continue to discover new, small-molecule therapeutic agents, an important paradigm shift to large-molecule, biopharmaceutical products as well as individualized medicine (advanced biotherapeutics) has been made possible due to new advances in the biotechnology and bioprocessing communities.
Originally focused on protein replacement and monoclonal antibody based therapies, the profoundly rapid development and production of new therapeutics such as cell and gene therapies and COVID-19 vaccines based on messenger-RNA technology has further expanded the market and the need for a skilled and knowledgeable workforce.
This expansion affects every aspect of drug development, including manufacturing techniques, analytical methods and regulatory processes.
Admission requirements
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