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Streamlining Clinical Trial Activations - Best Practice Approach
Mary Veazie
Apr 21, 2021 - 01:00 PM EDT
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2-Day Virtual Seminar Cleanroom, Microbiology and Sterility Assuran...
Charity Ogunsanya
May 10 - May 11 , 2021
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2-Day Virtual Seminar Vendor and Supplier Qualification Program for...
Joy L. McElroy
May 12 - May 13 , 2021
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2-Day Virtual Seminar Validation, Verification and Transfer of Anal...
Mark Powell
May 17 - May 18 , 2021
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2-Day Virtual Seminar FDA Audit, Quality Assurance Practices, Respo...
Kenneth Christie
May 20 - May 21 , 2021
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Streamlining Clinical Trial Activations - Best Practice Approach
Mary Veazie
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Coverage Analysis, Cost Estimation and Budgeting in Clinical Research
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Understanding and Implementing the EU Regulation for Initiating and...
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Trial Master File (TMF): FDA Expectations From Sponsors and Sites
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The 11 Must-Have Documents Of software Verification and Validation
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The Importance Of Protocol Deviations and Violations to Subject Saf...
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How to Make Efficient FDA-Compliant Clinical Protocol Amendments
Michael C Redmond
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