I am very pleased to recommend DQR MedTech LLC. I have worked with him on freelance basis over past two years. Though I have communicated with him over phone, mails, and virtual media yet I have known him/her as a competent professional with solid knowledge of EUMDR, CER, CEP, BER, BEP and excellent work ethics.

I got a chance to engage him since last two years to till date whenever we have an urgent priority task on CER, CEP, BER, and BEP. He offered to complete the task at the earliest and it was completed as promised. He has a strong sense of responsibility and attention to detail which helps our company to enhance its customer base due to the quality of work provided.

He has been a great talent within our team as on requirement basis. I have seen him grow as an excellent employee. I highly appreciate/recommend for him for his skills that can be utilized for long-term in our organization.

I have collaborated with DQR MedTech LLC on several projects for 2017/745, the EU Medical Device Regulations. DQR MedTech LLC completed Clinical Evaluation Reviews, Biological Risk Plans/Evaluations and Post Market Surveillance for four (4) of our product families. DQR MedTech LLC is knowledgeable of the requirements and brings a practical understanding of the regulations, at a reasonable price point. We continue to engage DQR MedTech LLC as we seek to bring additional products to the EU marketspace.