Mikael has more than 30 years experience in the Managment of international companies and 20 years experience in the Pharma field. His special areas are Pharma research and Pharmaceutical development including all preclinical studies. During the past 10 years he was in charge of Quality Manger and Responsible Person (RP / FvP).
Now he is running AaMEDI GmbH and several management consulting tasks, quality management projects nd several special projects.
John has more than 30 years experience in the pharma industry as Medical Director, University lecturer at ETH, Quality Manager, Quality Person, Responsible Person and QPPV. His special areas are Medical Imaging (MRI), Pharma Quality and safety, GMP and GDP as well as pharma logistic. He takes part in congresses and is a regular speaker in different events around the world. At AaMEDI he participates several special projects.
Kalevi has 40 year experience in the pharma filed as Chief Physician, Professor, Managing Director of several Biotech companies, His Medical specialities include Nuclear Medicine and Molecular Radiotherapy (Theranostics), Pharmaceutical Medicine, Medical Imaging (CTI).
He has organized world congresses around the globe and is a regular speaker in different events around the world.
At AaMEDI he participates in several special projects, especially in development of nanoparticles for Medical Imaging.
Pekka has more than 25 experise in the pharma industry in the area Global Regulatory Affairs
- Regulatory affairs filing, Variations and Submission of files
- Adaptation to the Swiss requirements
- Medical information / leaflets
- Packaging related questions
- Price negotiation for Switzerland
- Responsible Person, QPPV
Conrad has more than 20 years of professional experience in the fields of business development in Life Science, Comparative Medicine, Pharmaceuticals, Medical Devices including planning, construction and management of laboratories with responsibility for budget and staff.
He is a member of "Member of the German delegation of experts for harmonizing of ISO norms 10993 for the assessment of biocompatibility of medical devices".