Rexpharma Limited (EU QP Service)

Rexpharma is an agile, Irish pharmaceutical services company trusted to provide market access services for US, Canadian, UK, & Japanese clinical sponsors. Our responsive QPs deliver batch certs for your IMP as part of importation into Europe/ROW and release it onwards to your clinical trials. We provide this virtual QP release/batch certification service to Clients as a platform to get your IMP into your EU clinical trials. Also provided are QP declarations for your New Drug Applications, and an extensive range of audit types from QP, RP, PAI, PLI, due diligence for a new supplier, internal audits, and mock audits. A significant issue for small-to-medium enterprises is that they often do not the service level needed from their existing contract QP team in the EU. We have built our business service with this in mind. Our QPs will sit on your project calls with you and provide EU QP oversight & support. Your team members will have direct access (phone & email) to their Rexpharma EU QP for any issues to be resolved. We have in-house pedigree of launching clinical and commercial products in Europe and North America. With over 40 years’ experience, our founders have huge exposure to a wide range of drug doses, formulations, and routes of administration. Email us at info@rexpharma.ie for more information on EU IMP Batch Certification and for QP support on your project today.