Resource Center

Find the latest content and resources from our team of experts to keep you in the know for all things quality and regulatory in the life science industry.

Ending a Recall

Ending a Recall

All things must inevitably come to an end, including a medical device recall. Whether voluntary or FDA mandated, ...
EU MDR: Importers

EU MDR: Importers

The new EU MDR 2017/745 is complex, to say the least. Depending on a company’s relationship to the medical device ...
The FDA, CBD, and OTC Drugs

The FDA, CBD, and OTC Drugs

‌  When making a new product, whether that product is a drug, a medical device, or a combination product, ...
QMS For CBD Companies

QMS For CBD Companies

‌  Around the world, there are different regulations regarding the cultivations, manufacture, and sale of ...
EU MDR: Distributors

EU MDR: Distributors

‌  The new European Union regulation for medical devices, EU MDR 2017/745, went into effect only recently ...

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