Eric Che, MRPharmS
Technical Director and Qualified Person
Eric has worked in the pharmaceutical sector over the last 15 years since completing his pharmacist training in the NHS. Eric is also an eligible EU Qualified Person and has been responsible for supply chain audit oversight and batch release for clinical and commercial products.
During this time, he has worked with a broad range of sterile and non-sterile dosage forms including orphan products as well as time critical sterile and veterinary products. Eric has held leadership roles in quality delivering green field manufacturing facility design project, GMP licence applications and building a brand-new quality teams.
Eric has always held the belief that there would be an opportunity to leverage on his knowledge and experience in building something special. He was fortunate enough to have come to know Peter who shared a similar background but more importantly aligned in embracing challenges with an inspired and forward-thinking approach. RenaClinical was founded based on this shared value of both co-founders offering a tailored and responsive clinical trial manufacturing services to Sponsors with a diverse set of requirements.
Peter Mollison, MRPharmS
Quality Director and Qualified Person
Peter has over 15 years’ experience working in the pharmaceutical industry. He qualified as a pharmacist in 2004 and worked at the Institute of Cancer Research on a number of pharmacogenomic & drug discovery projects. After working within the Royal Marsden Hospital, Peter moved into commercial and clinical Sterile & non-sterile production roles within NHS & commercial organisations.
Since 2009 he has worked within Quality in commercial and non-commercial organisations covering a wide range of dosage forms including radiopharmaceuticals & ATMPs. Peter gained Qualified Person status in 2014 and performed commercial and non-commercial batch release for large and small-scale pharmaceutical organisations across the EU. He continued to work within the pharmaceutical industry as a consultant for a number of projects including new facility builds, FDA remediation, training and QMS design & implementation.
Peter was fortunate to meet Eric on a training course in 2008. After working together for the following 6 years Peter and Eric decided to establish their own clinical trial manufacturing company and founded RenaClinical Ltd in 2013. RenaClinical’s aim was to provide a tailored and flexible clinical trial manufacturing service to a wide range of Sponsors and Clients.