Berit Gehrke

As an experienced employee in practice administration with a focus on quality management and medical device technology, my goal is to support companies with legally compliant documentation. With my 5 years of experience in practice purchasing and my qualifications as a representative for medical device safety (§ 6 MPDG) as well as a safety representative, I am familiar with the regulatory requirements.

My offer for your relief (100% home office):

Creation and revision of procedural instructions (SOPs) and QM manuals.

Support with documentation according to MPDG and ISO standards.

Structuring and maintaining technical documents. Furthermore, I have practical experience in the fields of hematology/hemostasiology, clinical chemistry, and IVF/andrology.

I offer you precise writing and sound expertise for your compliance. I look forward to your message for project-based collaboration!

Practical work in hematology and special collection, manual microscopy, blood collection from the vein and finger