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Uventia Global

In order to avoid contamination of the product, robust cleaning procedures must be performed. Our online meeting facilitates peers’ reflection and discussion on approaches to establishing and revising CV programs to meet regulatory requirements, verifying CV protocols and preventing ineffective or incorrect approaches to cleaning validation programs, risk based cleaning validation, selecting the right equipment/cleaning procedure combinations, testing for API residues and calculating residue limits, considerations on combining cleaning and sanitization, finding and developing practical analytical methods and sampling procedures.

Email: info@uventia.com

QRM, Cleaning Validation, Containment, Bioprocessing, Bioproduction, Aseptic, GMP, Regulatory Affairs, Quality Assurance, QA, Risk Management

Pharmakologie und Arzneimittelentwicklung,    Biotechnologie