Kerstin Lundberg, CRM

Clinical trial management, phase II – IV, including applications to ethical committees and regulatory authorities and co-ordination of multi-national studies.

Experienced in working in accordance with international standards (ICH) and good clinical practice (GCP).

Long experience from drug development and more than 10 years of clinical trial management from both the pharmaceutical industry and CRO’s.

Tel. no: +46 70 229 9789

E-mail: kerstin.lundberg@megera.se