Yahoo Finance

Pharma & Biotech Computerized Systems Validation, Data Integrity & Cloud Computing Training Seminar (Dec 9th - Dec 10th, 2025)

Dublin, Nov. 07, 2025 (GLOBE NEWSWIRE) -- The "Computerized Systems Validation, Data Integrity & Cloud Computing In Pharma & Biotech (Dec 9th - Dec 10th, 2025)" training has been added to ...
Mena FN

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 ...

(MENAFN- GlobeNewsWire - Nasdaq) Dublin, Jan. 18, 2024 (GLOBE NEWSWIRE) -- The "Computerized Systems Validation, Data Integrity & Cloud Computing In Pharma & Biotech" training has been added to ...
Yahoo Finance

Computer System Validation Boot Camp : A 5 Day Complete Immersion in the Validation Process ( August 23 – 27, 2021) - Worldcomplianceseminars.com

The “Computer System Validation Boot Camp” seminar has been added to worldcomplianceseminars.com offering. RALEIGH, N.C., July 13, 2021 (GLOBE NEWSWIRE) -- World Compliance Seminars (WCS), a leader in ...
Business Wire

3 Day Online Computer System Validation for Cloud and COTS Applications Training Course (March 3-5, 2023) - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Computer System Validation for Cloud and COTS Applications-Live Online Training" training has been added to ResearchAndMarkets.com's offering. Advancements in technology ...
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

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 ...