VANCOUVER, British Columbia--(BUSINESS WIRE)--Elevated Signals, the manufacturing execution system (MES) for the cannabis industry, today announced it is GMP-ready, following third-party validation ...

Incorporating Q8, Q9, Q10 into good manufacturing practices (GMP), guidance on process validation, health based exposure limits covering cleaning validation and computerized system validation are the ...

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 ...

EMA's work plan emphasizes supply chain integrity, product quality, and new manufacturing technologies' impact on the supply chain. Revised GMP guidelines include updates to documentation, digital ...

Burlingame, June 12, 2023 (GLOBE NEWSWIRE) -- According to Coherent Market Insights, global computer system validation market is estimated to be valued at US$ 3.39 billion in 2022 and is expected to ...

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 ...

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 ...

Dublin, Aug. 25, 2025 (GLOBE NEWSWIRE) -- The "Digital Validation Demystified - GAMP? 5 2.0 and CSA Integration" training has been added to ResearchAndMarkets.com's offering. This course equips you ...

EU good manufacturing practice (GMP) Annex 11 regulation on computerized systems has been effective since 1992. 1 Following the data falsification uncovered at Able Laboratories in 2005, 2 many data ...