Medical devices as well as In vitro diagnostic medical devices are products that require a customized approach. Clinmark can assist clients in developing a clinical development strategy for a medical device, as well as pre-market clinical trials, clinical evaluations and post-market follow-up by providing:
- knowledge of regulatory requirements and standards related to clinical trials
- our expertise in several therapeutic areas i.e., oncology, neurology, ophthalmology and many others
- access to clinical trial sites worldwide