The participants have the opportunity to be trained in Cleaning Validation, with contents explained and presented in detail, with the application of risk analysis, as a relevant part of the GMP of the Pharmaceutical Industry, and to understand in depth all the related aspects, with these aspects of quality in the manufacture of medicines or Standards of Correct Manufacture of medicines, and the growing demands derived from FDA-EMA-PICs guides and their audits. This course will be held from October 3 to December 2, 2022.
Please use the folling links to access the course you can access the course sheet and calendar.
This course is held in English, if you want to access the Spanish version, please click here. Contents are the same.
Please contact ATEC+ID, or send an e-mail, or just go back to the blog, we will be pleased to provide you with more information.
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