Royal Society of Chemistry

2-day In-person Seminar on Validation and Part 11/Annex11 Compliance of Computerized Analytical Systems and Data at Singapore

Analytical equipment should be qualified and computer systems should be validated to demonstrate suitability for the intended use. Electronic records must comply with FDA Part 11 and EU/PICS GMP Annex ...
Yahoo Finance

Virtual FDA Compliance and Clinical Trial Computer System Validation Course 2024: Pre-approved by RAPS as Eligible for Up to 12 Credits Towards RAC Recertification

Dublin, Jan. 17, 2024 (GLOBE NEWSWIRE) -- The "FDA Compliance and Clinical Trial Computer System Validation Course" training has been added to ResearchAndMarkets.com's offering. The FDA governs the ...
Chromatography Online

The Answer’s AI. What’s the Question?

AI refers to a machine-based system and ML refers to a set of techniques that can be used to train AI algorithms (2) so ML ...
PharmiWeb

3 Day Virtual Computer System Validation (CSV) Training Course | Streamlined Validation with a Focus on Risk-Based Approaches (Sept 23rd - Sept 25th, 2025) - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Computer System Validation (CSV) Training Course (Sept 23rd - Sept 25th, 2025)" training has been added to ResearchAndMarkets.com's offering. The attendee will learn ...
Royal Society of Chemistry

Utilizing Good Requirements as a Foundation for the Effective Validation of PDMA-related Computerized Systems - Webinar By GlobalCompliancePanel

Computerized systems can be a boon to the Sales and Marketing group of an organization that falls within FDA regulatory authority. By automating, tracking, and reporting on thousands of sample product ...
Business Wire

ValGenesis iRisk Selected to Support Safer, Compliant Vaccine Production and Distribution in Brazil

SANTA CLARA, Calif.--(BUSINESS WIRE)--ValGenesis Inc., the market leader in enterprise validation lifecycle management systems (VLMS), announced today that a prominent Brazilian government entity, a ...