Dr. Philippe Thiel is an expert in clinical evaluations and relevant technical documentation, in accordance with the MDR, MDCG, CS, and MEDDEV 2.7/1 Revision 4. Dr. Thiel supports manufacturers throughout the entire process, including clinical strategy, development plans, literature reviews, preparation of clinical evaluation reports, PMCF planning, integration of PMS, and writing of SSCP. He covers planning, implementation, and also process design. Dr. Thiel's expertise is grounded in a doctorate in the natural sciences, extensive research experience in biotechnology, and over ten years of practical experience in regulatory affairs and clinical affairs.
Blog Post by Dr. Philippe Thiel - Expert Clinical Affairs
