Monetary benefits will outweigh the hassle of batch record harmonization, says Siegfried Schmitt, principal consultant at PAREXEL. Q: Our company recently acquired several new production sites in ...

As a part of international regulatory standards of GMP, pharmaceutical industries are required to maintain documentation of the entire manufacturing process and batch ...

Dublin, Sept. 30, 2024 (GLOBE NEWSWIRE) -- The "Efficient Batch Record Design and Review" training has been added to ResearchAndMarkets.com's offering. This online training is designed for ...

Lonza will unveil its next-generation electronic batch record execution platform, the MODA-ES™ Software Platform, at the Cell & Gene Therapy Manufacturing Forum from 13-15 November 2018, in London (UK ...

Dublin, June 12, 2023 (GLOBE NEWSWIRE) -- The "Efficient Batch Record Review and Product Release Training" webinar has been added to ResearchAndMarkets.com's offering. Most Regulatory Agencies require ...

DUBLIN--(BUSINESS WIRE)--The "Efficient Batch Record Design and Review" training has been added to ResearchAndMarkets.com's offering. This online training is designed for professionals in the ...

Written procedures are to be established and followed for a time efficient and clear evidence of the quality related elements during the review and approval for release, including packaging and ...