About us

PharmDr. Renáta Veselá

I graduated in pharmacy at the Faculty of Pharmacy of Charles University in Hradec Kralove. After completing my Master's degree in 2003, I continued my studies remotely and during the following year I passed the state rigorosum examination with the title of PharmDr.

My first short work experience was at the State Institute for Drug Control, where I worked as an analytical chemist. After a few months, I was approached by pharmaceutical company Zentiva (later Sanofi), where I joined the newly opened trainee program. After a one-year rotation in all departments at Zentiva, I chose to work in the R&D department as Formulation Specialist . Here, for the next seven years, I participated in the development of generic drugs (tablets, capsules and gels) from the laboratory phase to market launch. Gradually I also gained experience in quality, project management, purchasing and people management.

The turning point in my life was starting a family and the desire to return to the quieter, native Havlickuv Brod.

So in 2012 I moved with my family from Prague and chose to work for Arrow International / Teleflex. I completely changed my field and started to focus on the quality of medical devices. I passed my first auditing certification and the next 7 years of my professional career were marked by auditing of suppliers around the world. In 2016, I additionally took on the challenge of leading an entire quality team of nearly 50 people.

In 2019, I decided to go independent and pursue auditing full time. I have established contacts with multinational medical device and pharmaceutical manufacturers and several certification bodies, for which to date I have performed more than 300 supplier, certification and internal audits worldwide as a Certified Lead Auditor.

I later expanded my business to include consulting for medical device and pharmaceutical manufacturers and quality manager training.

With the increasing volume of assignments, I am expanding my network of collaborators with other auditors and consultants. Today, I am able to offer my customers a team that covers all phases of the medical device or drug lifecycle in the area of quality.