Clinical Operations

D-TARGET`s medical device professionals team is capable to manage even the most complex research projects to successful conclusion. Prepared to act on very short notice and resolve any issue with pragmatic solutions together with our clients, D-TARGET offers industry professionals and clinical experts with the depth knowledge and experience

neccessary to effectively manage any situation that may arise throughout your clinical trial.
The D-TARGET employed, multi-lingual, medical device CRAs are located throughout Europe and NA. Our CRAs or “monitors” are sourced from a clinical/nursing background and are familiar with the often present hierarchy of the hospital, particularly within the Operating Theater and Catheterization laboratory settings. D-TARGET CRAs have prior direct experience with medical devices and their application and are thoroughly trained on their roles and responsibilities in response to anticipating problems relating specifically to medical device trials. They can also provide technical support to sites if needed

Our industry professionals and clinically trained Project Managers focus entirely on medical device trials

Services

Project Management
Protocol Development
Feasibility
Site Identification and Selection
Site Qualification
Investigator Contract Negotiation
Regulatory Document Management
IRB/EC Submission
Investigator Meeting Preparation
Site Initiation
Clinical Monitoring
Site Management
Patient Recruitment Support
Investigator Grant Management
Trial Master File Management
Vendor Management