Always service-oriented, I provide helpful, constructive solutions.
Pharmacovigilance is a dynamic and highly changeable field. Constant updates and amendments to existing legislation make every new assignment a challenge. In my years of experience working for a clinical research organisation, as well as for several small and large pharmaceutical companies, I handled many different kinds of assignments, from newly established pharmaceutical companies and companies that were issued a new license for a product, to post-marketing release of pharmaceuticals.

By being pragmatic, I achieve efficient and practical results.
I ensure purposeful, targeted solutions that are workable for every department within a company. Much of my experience has been in CAPA (Corrective Action, Preventative Action) and subsequently deciding upon an appropriate approach. Once this has been established and the company is inspection proof – it’s time to get to work without further delay!

My ambition lies in overcoming challenges.
Establishing order and ensuring developments in EMA regulations and legislation are correctly taken on board by a company’s PV department are some of my key activities as a consultant.

Orderly, structured, accurate and methodical support in the implementation of improvements to Pharmacovigilance.
I am able to elucidate where the obstacles to the smooth running of operations are, manage and guide audits and inspections as well as aid in the implementation of CAPA processes.