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3 Hours Virtual Seminar: Japan Regulatory Compliance Requirements ...
Robert J. Russell
Jun 26, 2019 - 01:00 PM EST
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Vendor Qualification - How to Design and Implement An Efficient and...
Todd Graham
Jun 27, 2019 - 01:00 PM EDT
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State of the Art: Recommendations for writing a thorough SOA and bu...
Maria Sanchez
Jun 27, 2019 - 01:00 PM EDT
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Validation, Verification and Transfer of Analytical Methods (Unders...
Mark Powell
Jun 27 - Jun 28 , 2019
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Efficient and Effective Batch Record Reviews to Improve your Proces...
Danielle DeLucy
Jul 5, 2019 - 01:00 PM EDT
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21 CFR Part 11 and Annex 11: What You Need to Know to Pass the New ...
David Nettleton
Jul 10, 2019 - 01:00 PM EDT
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Trial Master File (TMF): FDA Expectations From Sponsors and Sites
Marina Malikova
Jul 11, 2019 - 01:00 PM EST
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GxP/GMP Requirements and its Consequences for Documentation and Inf...
Eleonora Babayants
Jul 23, 2019 - 10:30 AM EDT
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SOPs for FDA-Regulated Industry -Best Practices to Withstand FDA Ex...
Peggy J Berry
Jul 25 - Jul 26 , 2019
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Clinical Trial
Clinical Data Management (FDA E6 GCP Guidelines)
Elaine Eisenbeisz
Aug 1 - Aug 2 , 2019
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Clinical Trial
Quality Control Laboratory Compliance - cGMPs and GLPs
Kelly Thomas
Aug 15 - Aug 16 , 2019
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Clinical Trial
Biostatistics for the Non-Statistician
Elaine Eisenbeisz
Sep 5 - Sep 6 , 2019
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Hospital & Healthc..
3 Hours Virtual Seminar: Japan Regulatory Compliance Requirements ...
Robert J. Russell
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Pharmaceutical
Vendor Qualification - How to Design and Implement An Efficient and...
Todd Graham
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