RenaClinical was founded to provide tailored and responsive clinical trial manufacturing & distribution services to Sponsors with a diverse set of requirements.

RenaClinical has a wide range of manufacturing and packaging capabilities within their MHRA & HPRA approved facilities

Our QPs have a wide range of knowledge & experience to provide expert regulatory & CMC advice to clients

RenaClinical's depots in the UK, Ireland, Spain, Poland & Australia offer global distribution solutions

Our MHRA and HPRA approved facilities enables seemless IMP importation into the UK and EU

With our regulatory knowledge & expertise we offer support with your clinical trial submissions and provide advice on MHRA, EU and US regulatory & supply chain requirements

RenaClinical prides itself of providing an end-to-end project management service to all clients to ensure project milestones are achieved

Our external training program is run and managed via RenaClinical QPs. Training can be tailored to the needs of the client in order to achieve the best possible learning outcomes

RenaClinical can provide a wide range of other supporting services to ensure your clinical trial needs are met

Visit our website to find out more!