Dublin, Dec. 01, 2021 (GLOBE NEWSWIRE) -- Less than two weeks to register for the "Computer System Validation (CSV) Training" training course has been added to ResearchAndMarkets.com's offering. This ...

Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation. You’ll learn about what processes needed to be ...

Dublin, April 20, 2023 (GLOBE NEWSWIRE) -- The "Computer System Validation ( CSV) 3 Day Virtual Seminar" training has been added to ResearchAndMarkets.com's offering. This course is designed to ...

This article provides a historical review of computer validation in the pharmaceutical industry within the last three decades, evolving from the early years' initial concept and approach to today's ...

Dublin, June 29, 2021 (GLOBE NEWSWIRE) -- The "6-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, ...

For laboratories that operate within a quality management system, compliance with global standards such as ISO 9001, ISO 13485, ISO 17025, ISO 15189, GxP, and other country-specific regulations ...

All sectors of manufacturing are under continual pressure to bring new products to market quicker, stealing a march on the competition and maintaining their revenue stream. All sectors of ...

Syngene, a world-leading manufacturer of image analysis solutions, has announced that it has produced new software and validation information for its Dyversity, G:BOX and GeneGnome range of image ...

Quality and reliability are essential in pharmaceutical manufacturing. To ensure compliance and high standards are consistently met, the Installation Qualification (IQ), Operational Qualification (OQ) ...

DUBLIN--(BUSINESS WIRE)--The "6-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices)" webinar has ...