Based on a decade of experience with clinical quality services provided to external clients, Addomed can develop and follow a complete auditing programme as well as only particular auditing services.
Clinical system and procedure development
Addomed follows its ICH and EU Directive compatible SOPs but is able to operate also under the client’s Standard Operating Procedures (SOPs). QA system ensures that required quality level of tasks and results is attained during performance of clinical trials and other activities of the company. The basis is given in Quality Manual.
Clinical operation management
Working with different pharma companies and CROs (Actelion, KCR, BI, GSK, Jansen Cilag, Chiltern Sandoz (Lek)) and considering different monitoring strategies we are able to plan an intelligent and effective project specific concept which fits your needs.
Addomed provides full data management services for all types of studies – medicinal products and drugs, medical devices, from routine phase I trials through to large and complex phase III trials, as well as non-interventional studies.
Training courses can be customised to suit individual client needs. Addomed is ready to share its long-term experience in clinical research either with the beginners in this area as well as with the experienced members of the trial teams.