Client Voices
Some clients choose to share their experience publicly on LinkedIn after our projects. Others have shared their feedback directly with me. Here's what they've said about working together on Clinical Evaluations, PMCF planning, and MDR compliance.
LinkedIn Recommendations
These testimonials were shared publicly by clients on LinkedIn — without me asking for them. They reflect real experiences from Clinical Evaluation and regulatory compliance projects across different device types and company sizes.
Client Feedback
Additional feedback from clients I've worked with on Clinical Evaluations, PMCF studies, and MDR transition projects.
"Katharina's dedication to precision and accuracy in her medical writing is unmatched.
She consistently impressed us with her ability to satisfy our needs, meet stringent timelines and exceed our expectations. Working with Katharina was a pleasure because of her expertise and clear and friendly communication, and we highly recommend her services to others in need of a skilled and passionate medical writer ."
She consistently impressed us with her ability to satisfy our needs, meet stringent timelines and exceed our expectations. Working with Katharina was a pleasure because of her expertise and clear and friendly communication, and we highly recommend her services to others in need of a skilled and passionate medical writer ."
Nicolab's team
Medical Device Software Company, The Netherlands
"Katharina has been a great asset to our team and instrumental in our MDR submission. She prepared high quality clinical documents on time and supported us with strategic decisions. Katharina is a fantastic medical writer, well-tuned into the latest regulatory updates, always responsive and willing to help. Combined with her strong clinical expertise, she is a valuable contributor to any team. It is a pleasure working with Katharina and would I recommend her wholeheartedly!"
Clinical Evaluator and Project Manager
International MedTech Company, Sweden
"Katharina’s work is detailed, clear, descriptive, and persuasive. For example, she has authored several comprehensive Overseas Clinical Data Analyses and Evaluations for the China National Drug Administration (CNDA).
She has reviewed and summarized the international literature for CNDA evaluations, researched the international guidelines and guidance documents, and written comprehensive gap analyses detailing the similarities and differences between the regulatory requirements and clinical data presented internationally and in China.
These types of documents, if written poorly, can be difficult and confusing; because she is an excellent writer, Katharina makes them concise, accurate, and readable."
She has reviewed and summarized the international literature for CNDA evaluations, researched the international guidelines and guidance documents, and written comprehensive gap analyses detailing the similarities and differences between the regulatory requirements and clinical data presented internationally and in China.
These types of documents, if written poorly, can be difficult and confusing; because she is an excellent writer, Katharina makes them concise, accurate, and readable."
Director Clinical Science
International MedTech Company, USA
Get in touch