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 facilitiesOur 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 EUWith our regulatory knowledge & expertise we offer support with your clinical trial submissions and provide advice on MHRA, EU and US regulatory & supply chain requirementsRenaClinical prides itself of providing an end-to-end project management service to all clients to ensure project milestones are achievedOur 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 outcomesRenaClinical can provide a wide range of other supporting services to ensure your clinical trial needs are metVisit our website to find out more!