Pharmaceutical
Masters program on eCTD Submissions of IND/NDA to the US FDA, EU an...
Peggy J Berry
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Efficient and Effective Batch Record Reviews to Improve your Proces...
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Hospital & Healthc..
Writing Effective sops for FDA and CLIA Regulated Companies
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Clinical Trial
How to Manage Your Suppliers in China and India During the COVID-19...
Christopher R DeVany
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Bioanalytical sample re-analysis, ISR and analytical re-analysis
Edward 'O' Connor
Price:Pharmaceutical
Scheduling and Conduct of Good Pharmacovigilance Practice Audits
Miranda Peguese
Price:Pharmaceutical
Effective Implementation and Management Of GMP Data Integrity
Danielle DeLucy
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How To Manage Impact Of Coronavirus (COVID-19) For Global Pharma An...
Danielle DeLucy
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Solving Statistical Mysteries - What Does FDA Want?
Ron Snee
Price:Pharmaceutical
6 Hours Virtual Seminar: Process Validation for Drugs and Biologics
Joy L. McElroy
Price:Pharmaceutical
MS Excel: Advanced Pivot Tables for Superior Data Analytics
Mike Thomas
Price:Pharmaceutical