On June 30th, Qualipharma offered a free webinar about the new version of ISO 14644-1-2 regulation and its implications and impact on the pharmaceutical sector.
To know all these details, we share the video of the webinar and the answers to different questions such as: Do you know how to define the corrective measures and the requalification actions if your clean rooms do not comply the existing regulations? Are you aware of all issues that have changed with the new edition of ISO 14644? Do you know about how the acceptance criteria have changed in order to verify if a room meets or does not meet its classification?
The experts Miguel Ruiz, GMP Engineering Consultant in Valtria and Jorge Frutos, Quality Director of Qualipharma, led this webinar.
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