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FDAnews Announces — Data Integrity for GMP/Postmarket Professionals: Core Requirements, Expectations and Challenges Virtual Workshop March 30, April 1, 2021


FDAnews Announces Data Integrity for GMP/Postmarket Professionals: Core Requirements, Expectations and Challenges Virtual Workshop March 30, April 1, 2021
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Can one’s data integrity controls withstand FDA scrutiny? Here’s how to stay compliant and avoid 483s or warning letters. Register today.
WCG FDAnews
Data Integrity for GMP/Postmarket Professionals:
Core Requirements, Expectations and Challenges
A Virtual Workshop Presented FDAnews and Cerulean Associates LLC
Tuesday, March 30 and Thursday, April 1, 2021, 10:00 a.m.-4:30 p.m. EDT
Is the FDA’s increasing scrutiny on data integrity producing a data migraine? One must establish internal competency and assessment programs; otherwise, one can expect to receive a Form 483 or warning letter. ....

John Avellanet , Department Of Justice , European Medicines Agency , Cerulean Associates , Postmarket Professionals , Virtual Workshop Presented , Core Requirements , Workshop Details , European Medicines , Press Release , துறை ஆஃப் நீதி , சிஇஆர்யுவ்எல்இஏஎன் கூட்டாளிகள் , மெய்நிகர் பணிமனை ப்ரெஸெஂடெட் , கோர் தேவைகள் , பணிமனை விவரங்கள் , ஐரோப்பிய மருந்துகள் , ப்ரெஸ் வெளியீடு ,