Access Training

Millipore’s world wide training facilities are located at our North American headquarters in Billerica, Massachusetts and European headquarters in Molsheim, France. We develop and provide state of the art courses containing core separation technology relating to actual biopharmaceutical manufacturing processes.

These courses range from 1-5 days and are designed to help biopharmaceutical manufacturers meet critical needs for process efficiency and cGMP compliance as per the U.S. Code of Federal Regulations 21 CFR § 211.259 and the EU Guide to Good Manufacturing Practice for medicinal products § 2.9.

A certificate is issued at course completion and records of attendance and laboratory data sheets are kept to address cGMP requirements. Additionally, Millipore courses count toward earning a college degree.

Regulations Regarding Training

The U.S. Code of Federal Regulations 21 CFR § 211.25:
Each person engaged in the manufacture, processing, packaging, or holding of a drug product shall have education, training, and experience, or any combination thereof, to enable that person to perform the assigned functions.“

The EU Guide to Good Manufacturing Practice for Medicinal Products § 2.9:
"Besides the basic training on the theory and practice of GMP, newly recruited personnel should receive training appropriate to the duties assigned to them. Continuing training should also be given, and its practical effectiveness should be periodically assessed. ...Training records should be kept".

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