Рет қаралды 6,777
Simin Hassannejad Tabasi and Pei-I Chu from the CDER Office of Pharmaceutical Quality discuss common drug product quality issues and CMC issues for manufacturing process and facility reviews.
Hassannejad Tabasi discusses ANDA applications related to Solid Oral Drug Products (SODP), identifies the most common areas of quality gaps in the ANDA submission, and possible resolutions.
Chu shares the key elements of process and facility review, commonly seen deficiencies for various dosage forms, and considerations for information to be included in the submission.
Learn more at www.fda.gov/dr...
_______________________________
FDA CDER’s Small Business and Industry Assistance (SBIA) educates and provides assistance in understanding the regulatory aspects of human drug products & clinical research.
Upcoming training and free continuing education credits: www.fda.gov/cd...
CDER SBIA 2020 Playlist: • 2020 CDER Small Busine...
LinkedIn: / cder-small-business-an...
Training resources: www.fda.gov/cd...
Twitter: / fda_drug_info
CDER small business e-mail update subscription: updates.fda.go...
Email: CDERSBIA@fda.hhs.gov
Phone: (301) 796-6707 I (866) 405-5367