Training is a vital element for ensuring that good practices are followed in medical device quality assurance, GMP and GLP. Manufacturers and laboratories can now take advantage of the on-site training that has been added to the MET shop. The packages are tailored to customer’s needs and cover:
Internal Quality Auditor for Medical Device Companies, Good Manufacturing Practice (21CFR Part 820)-Foundations, Good Laboratory Practice (OECD-FDA)-Foundations.
These training packages and much more support information can be found at the medical device solutions, sales site: sales.medical-engineering.co.uk
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Medical Engineering Technologies is here to help you get to market quicker with a fully validated medical device or production process. We provide engineering and scientific solutions exclusively to the medical device, biotech and pharmaceutical industries.
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