Investigating Out-of-Specification (OOS) Test Results in the Laboratory: FDA Guidance and Latest Expectations Webinar (ONLINE EVENT: September 30, 2024/ON-DEMAND)
18 sept. 2024 11h11 HE
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Research and Markets
Dublin, Sept. 18, 2024 (GLOBE NEWSWIRE) -- The "Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FDA Guidance and Latest Expectations" webinar has been added to ...
FDA Inspection Preparedness and Compliance Seminar: Information and for Tools Pharmaceutical, Biopharmaceutical, Biologics and Medical Device Professionals | ON-DEMAND
02 sept. 2024 10h46 HE
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Research and Markets
Dublin, Sept. 02, 2024 (GLOBE NEWSWIRE) -- The "FDA Inspection Preparedness and Compliance" training has been added to ResearchAndMarkets.com's offering. This is a practical, hands-on two-day...
Enhanced Validation Plans to Meet FDA Expectations and Mitigate Risk Seminar: Addressing GMP Deficiencies through Risk-Based Validation Strategies
02 sept. 2024 06h28 HE
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Research and Markets
Dublin, Sept. 02, 2024 (GLOBE NEWSWIRE) -- The "Master Validation Plan - The Unwritten Requirements" report has been added to ResearchAndMarkets.com's offering. Master Validation Planning...
Cutting-Edge FDA Inspection Preparedness Tactics Course (ON-DEMAND)
02 sept. 2024 06h12 HE
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Research and Markets
Dublin, Sept. 02, 2024 (GLOBE NEWSWIRE) -- The "FDA Inspection" training has been added to ResearchAndMarkets.com's offering. The course will go through what typically goes on during an FDA...
Risk Management of Raw Materials in a GMP Environment Course (ON-DEMAND)
02 sept. 2024 05h10 HE
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Research and Markets
Dublin, Sept. 02, 2024 (GLOBE NEWSWIRE) -- The "Risk Management of Raw Materials in a GMP Environment Course" training has been added to ResearchAndMarkets.com's offering. Risk management of raw...
21 CFR Part 11, SaaS/Cloud, EU GDPR Data Integrity and Privacy Compliance Webinar (ON-DEMAND)
09 juil. 2024 04h41 HE
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Research and Markets
Dublin, July 09, 2024 (GLOBE NEWSWIRE) -- The "Data Integrity and Privacy: Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR" training has been added to ResearchAndMarkets.com's offering.This 21...
FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers (ON-DEMAND COURSE)
27 juin 2024 10h01 HE
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Research and Markets
Dublin, June 27, 2024 (GLOBE NEWSWIRE) -- The "The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers" training has been added to ...
Writing and Enforcing SOPs for FDA-Regulated Industry Online Course: Best Practices to Withstand FDA Expectations
21 mai 2024 10h08 HE
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Research and Markets
Dublin, May 21, 2024 (GLOBE NEWSWIRE) -- The "Writing and Enforcing SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations Course" training has been added to ...
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions Training Course
14 mars 2024 13h54 HE
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Research and Markets
Dublin, March 14, 2024 (GLOBE NEWSWIRE) -- The "Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions Training Course" training has been added to ...
2 Day Virtual FDA Inspection Course: How to Prepare for, Host and Follow up to a Regulatory Inspection (12.0 RAC CREDITS)
18 janv. 2024 07h28 HE
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Research and Markets
Dublin, Jan. 18, 2024 (GLOBE NEWSWIRE) -- The "FDA Inspection" training has been added to ResearchAndMarkets.com's offering. The course will go through what typically goes on during an FDA...