Have questions or need support? Contact Rexpharma for a confidential call today. Our team is ready to assist you with your pharmaceutical certification and QP support needs
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Whether you're looking to start a new project or need assistance with an existing one, we're here to help you every step of the way.
Contact our technical team to discuss your project today
Contact Rexpharma today to learn how we can support your and launch your EU clinical trials program. Our experienced team is here to help you navigate the complexities of the EU market with ease.
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We are clinical specialists that provide small-to-medium size businesses access to the EU for their new/existing clinical trials. We do this by adding your drug(s) to our in-house license (IMP MIA) and our QPs get your products into trials by certifying for release in the EU/ROW.
We support your regulatory applications with in-house QP Declarations needed for your Clinical Trial Application/Variations.
We manage your supply chain and provide bespoke audit services to you company and supplier network to ensure EU compliance, as well as training and Quality/QP support on your projects.
We deal with everyone from one person & a molecule, all the way up to large corporate entities. We have structured our business to serve small-to-medium enterprises best.
This is readily accommodated, and part of our business model. Do reach out to learn more here.
We ideally will start the onboarding process 6-12 months out from when the Client needs QP certification. We do offer expedited onboarding and expedited certification/release services.
Our strategy is to list as many suppliers on our license as possible so we can expedite your onboarding. We expect initial onboarding to take 3-6 months depending on the complexity of your operations.