Our team of experienced and highly qualified experts has a clear focus and proven track record of successfully compiling Clinical Evaluation Reports according to the requirements of MEDDEV 2.7.1, MDD and the MDR. We cover a broad variety of products ranging from simple class I medical devices to class III implants and combination products.
Medical Mind is your competent partner for medical device clinical trials. We offer customised solutions from the planning stage to study management and publishing. Working side-by-side with your team, our streamlined services guarantee strict regulatory compliance and data integrity to provide high-quality clinical research, on time and within budget.
Medical Mind’s team members have up to 20 years of experience in the medical device industry covering all stages of product development from early R+D to market approval. Apart from clinical research, we offer the following expert services:
Our tailored services aim to guarantee product specific regulatory compliance throughout the complete life cycle.
Design, implementation and maintenance of quality management systems according to ISO 13485.
Development of intelligent strategies to establish the biological safety of your medical devices according to EN ISO 10993-1.