Teva receives warning letter over Actavis site
Celltrion confident in quality of biosimilars despite FDA 483
Sanofi begins work on succession plan; FDA issues warning letters to Lupin's US, India units | Radio Compass Blog
Teva catches break as warning letter looks to delay Momenta Copaxone generic | FiercePharma
India 2019 – R&D Highs, Compliance Woes And Other Lows :: Pink Sheet
Pfizer and Teva Reach $2 Billion Deal on Patent Spat
FDA Bans Imports From Teva's Hungary Plant Except Two Drugs in Shortage | RAPS
Celltrion slammed with US FDA warning at biosimilar site
Teva plant tagged with warning letter for issues making schizophrenia drug | FiercePharma
UPDATED: FDA Issues CLRs for Two Celltrion and Teva Biosimilars | BioSpace
FDA cites 'significant' sterility concern at Teva injectables plant | FiercePharma
/cloudfront-us-east-2.images.arcpublishing.com/reuters/CCBS56SBRRKUDM7JEVVE3UOQEE.jpg "Teva halts output at U.S. drug plant after FDA flags concerns | Reuters")
Teva halts output at U.S. drug plant after FDA flags concerns | Reuters
Teva partners with Just Biotherapeutics, ramping up biologics productivity - BioProcess InsiderBioProcess International
Teva Stops Production At US Plant After FDA Concerns: Report
FDA Keeps Brand-Name Drugs On A Fast Path To Market ― Despite Manufacturing Concerns | Kaiser Health News
Celltrion receives FDA 483 with 8 'manageable and correctible' observations - BioProcess InternationalBioProcess International
Analysis of FDA Infrared 483 Citations: Have You a Data Integrity Problem?
Aurobindo Receives Warning Letter After Form 483 :: Generics Bulletin
Biosimilar… but different: FDA tweaking nonproprietary name guidance - BioProcess InternationalBioProcess International
UPDATED: Teva's struggling sterile plant hit with FDA warning letter | FiercePharma
FDA Form 483 shows Pfizer repeating same mistakes at troubled fill-finish plant | FiercePharma
Adam Hricz - Associate Director, Commercial Supply Chain Hungary - Teva Pharmaceuticals | LinkedIn
angiotensin II receptor blockers (ARBs) - News, Articles etc. - European Pharmaceutical Review
Teva's struggling sterile plant hit with FDA warning letter - Skyland Analytics
Teva two: FDA approves Celltrion-made Herceptin biosimilar - BioProcess InternationalBioProcess International
Teva's rating cut to junk, Two Lupin facilities receive FDA warning letters | Radio Compass Blog
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