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Donatelle

Biorep Technologies Inc.

With a sole focus on designing and developing regulated medical devices, we have the regulatory registrations and certifications, in-house knowledge, global suppliers and vertically integrated process in place to bring your medical device from concept to launch. As a single source solution for your medical device development we reduce program risk, cut development costs and meet your go-to-market timeline.

Biorep is ISO 13485 Certified and FDA Registered. As a full-service development firm, Biorep has an exclusive focus on medical products and over 20 years of experience developing medical devices.

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