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Seminar on DI and Part 11
Seminar on FDA Inspection
Seminar on Supplier Mgmt
GMP Master Class
Seminar on CSV DI for Clinical Trials
Seminar on CSA vs CSV
Seminar on Vendor Qualification
CSV Boot Camp
Seminar on SOP Writing
Seminar on Verification and Validation
Seminar on Technical Writing
Seminar on Analytical Method Validation
Seminar on QC Labs
Seminar on Analytical Instrument Qualification
Seminar on Internal Audits
Process Validation Training Course
Seminar on Lab Compliance Documentation
Seminar on Complaint Handling, MDR and Recalls
Seminar on Human Error Prevention
Seminar on FDA Inspection Recording
3-Day Annual GMP Master Class for 2022
Sorry, registration has ended.
Date:
5/2/2022 11:00 PM
Location:
Online Event
+1-416-915-4458
+1-416-915-4438
info@eventura.world
