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The Montrium Blog

The most helpful and thought-provoking ClinOps content from our writers on the front-lines of the life sciences industry

There is a typical reaction when doing research around what regulations you need to account for. Most tend to focus their efforts towards the FDA’s 21 CFR Part 11 due to its international reach, however, if most of your efforts are focused in Europe, you’ll want to be mindful of some of the guidelines to adhere to over on that side of the pond.

Regulations Standards

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