Bosilka Kocare

Bosilka Kocare

Senior Specialist Regulatory Affairs


Bosilka is experienced Regulatory Affairs Specialist with a demonstrated history of working in the wholesale industry. Skilled in Regulatory Affairs, Pharmacovigilance, Clinical Trials and strong legal professional background with a Master’s Degree focused in EU Regulation.

She has gained her six-year Regulatory experience supporting and acting as Regulatory Affairs Associate and QPPV for respective Pharma companies such as Pfizer, Mylan, Berlin Chemie, Octapharma and many more.

Currently, she is working as a Senior Specialist Regulatory Affairs in PharmaLex Bulgaria and mainly supporting as global point for regulatory matter per Bayer CH project.

Her dissertation in Pharmacovigilance and managing safety data in Clinical trials also led her to sustainable experience in Clinical trials and international differences in regulations on SUSARs.

Other speakers in 2020

Dobrin Svinarov


Prof. Dr. Dobrin Svinarov, MD. PhD, Dr. Med Sc

Head of Clinical Laboratory and Clinical Pharmacology at Alexandrovska University Hospital / Chairman of the Department of Clinical Laboratory and at the Faculty of Medicine, Medical University of Sofia / President of the Bulgarian Society of Clinical laboratory
Liliya Evtimova-Tichev

Bulgaria, The Netherlands

Liliya Evtimova-Tichev

Validation/Qualification Engineer for Quality Assurance
Lonza, Netherlands
Skip to content