Yahoo Finance

2 Day Online Pharma & Biotech Computerized Systems Validation, Data Integrity & Cloud Computing Course: Pre-Approved by RAPS as Eligible for Up to 12 Credits Towards RAC ...

Dublin, Jan. 18, 2024 (GLOBE NEWSWIRE) -- The "Computerized Systems Validation, Data Integrity & Cloud Computing In Pharma & Biotech" training has been added to ResearchAndMarkets.com's offering.
Yahoo Finance

2 Day FDA Pharma & Biotech Computerized Systems Validation, Data Integrity & Cloud Computing Webinar: Explore Compliance Strategies for COTS and Cloud Software (ONLINE EVENT ...

Dublin, June 25, 2025 (GLOBE NEWSWIRE) -- The "Computerized Systems Validation, Data Integrity & Cloud Computing In Pharma & Biotech" has been added to ResearchAndMarkets.com's offering. The seminar ...
akm

The EEC has adopted Guidelines on Data Integrity and Validation of Computerized Systems

The Board of the Eurasian Economic Commission has adopted Guidelines on Ensuring Data Integrity and Validation of Computerized Systems. The manual contains recommendations for pharmaceutical ...
JD Supra

FDA’s Draft Computer Software Assurance Guidance Changes the Game for Quality System and Production Software Validation

On September 13, 2022 the Center for Devices and Radiological Health (CDRH) and the Center for Biologics Evaluation and Research (CBER) jointly released a new draft guidance document titled “Computer ...
Business Wire

Research and Markets: E-Learning Course: IT Use and Analytical Validation (Certified) - The Fundamentals of Computerized Systems Validation Are Explained and How it Works

DUBLIN--(BUSINESS WIRE)--Research and Markets(http://www.researchandmarkets.com/research/7989d0/elearning_course) has announced the addition of the "E-Learning Course ...
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 ...