Dr. Lars Dahms, QA and RA Manager

Dr. Lars Dahms has been an expert in the fields of biocompatibility, sterilization, and validation for over a decade, with deep expertise in both regulatory and operational aspects.

He prepares expert opinions and reports for the biological and toxicological hazard and risk assessment of medical devices, plans the testing strategy, and interprets data from chemical characterization. He also provides support in all areas related to ensuring the sterile and hygienic state of a medical device, including sterilization validation, final cleaning, and packaging validation.

As a trainer, Lars Dahms conducts seminars on biological safety and sterilization for medical device manufacturers, pharmaceutical companies, regulatory authorities, and notified bodies, through organizations such as the qtec Academy, TÜV Rheinland, and the DIN Academy.

What matters most to him as a speaker:
“As regulatory requirements increase, so does the need for high-quality training. In my seminars, I aim to guide participants, explore challenges in group discussions, and ensure that attendees benefit from both our expertise and the knowledge shared within the group.”