MD. Ph.D. Consultant Regulatory Affairs/Business Developer Asia

In October 2007, Chongde Luo, MD. Ph.D. joined Kinesis Pharma B.V. as Consultant Regulatory Affairs and Business Developer Asia. In this first position, he provides consult to different pharmaceutical companies in EU regarding all aspects of regulatory affairs, including clinical issues for drug development. He prepares regulatory documents, including clinical overviews for chemical medicines and traditional herbal products. In the second position, he is involved in business development in Asia. He is also intermediate in a Quality Assurance project of Kinesis Pharma to upgrade the quality level for a laboratory in China to obtain OECD-GLP accreditation.

Before joining Kinesis, he worked as Clinical Assessor in the Dutch Medicines Evaluation Board (2006-2007), giving him knowledge on Regulatory Procedures and Guidelines on clinical studies.

Dr. Luo obtained his Ph.D. degree in 2005 at the Neuroscience Institute of the Erasmus University Medical Centrum, Rotterdam, The Netherlands.

He had worked as a specialist in an academic hospital in Nanjing, China for 15 years. During his time in the medical school, he studied Western Medicine and got training of Traditional Chinese Medicine as well. His unique and broad experiences lead to fulfilling his task adequately in the field of interpretation of these two medicines.