Pharmatory offers wide range of R&D services tailored for drug discovery and development companies ranging from small virtual human and veterinary companies to medium size and global pharma companies. Our service palette includes route scouting, lab scale syntheses, analytical support and pilot scale cGMP manufacturing of key intermediates and APIs.
Pharmatory is capable of manufacturing GMP batches from milligram scale to tens of kilograms, making Pharmatory a perfect partner also for orphan drug and veterinary companies.
Pharmatory has been routinely inspected since 2001 by the European Medicines Agency and recently also by the FDA, making us a reliable partner for pharmaceutical companies. Inspections are also frequently carried out by our customers. Pharmatory quality control and assurance is an independent unit of 6 people within the company, dedicated to achieving the highest quality of all operations. They support the development and manufacturing teams throughout the project. They are also responsible for maintaining the SOP system of the company and managing several audits every year. Process development, batch documentation (equivalent to CMC documentation) and cGMP QA/QC management are standard procedures. Our QC/QA team can also help to determine the cGMP requirements together with the customer based on the needs of each project.
Health & Life Science, Life Science, pharmaceutical