Clinical investigations

We focus on first-in-man studies and post-market clinical follow-up data collection. Based on our experience we will come up with an efficient solution to get your device to market. We like to keep things simple, while never losing sight of quality. Our goal is to build balanced partnerships with clients, to meet critical goals, timelines and deliverables.  

We provide full-service CRO activities or separate services, including:

Regulatory & Medical Writing
  • Study Design & Protocol Development
  • Regulatory Submissions and Approvals
  • Investigator Brochure Development
  • Informed Consent Form Development
  • Writing of Clinical Investigation Report
  • Regulatory support as described under “Clinical Evaluation”
Data Management
  • CRF and Database build
  • Data Validation and Cleaning
  • Data Visualization
  • Data Lock
Clinical Operations
  • Site Qualification and Selection
  • Site Start-Up and Management
  • Monitoring and Close-Out
  • Project Management
  • Vendor Management
Safety Management
  • Medical Monitoring & Review
  • Regulatory notifications
  • DSMB/CEC Set-up and Management

Clinical evaluation

The MDR requires that clinical data is generated, collected and analyzed throughout the medical device lifecycle. Very often this process is only initiated while the clinical investigation already started. Clinical evaluation should be the starting point of doing a clinical study, as this process defines the questions to be answered and the data needed. Therefore, we encourage our clients to initiate clinical evaluation at an early product development phase, often during pre-clinical testing. Amongst others, our services include the joint development of:

  • Clinical Development Plan
  • Clinical Evaluation Plan
  • Clinical Evaluation Report
  • Post-Market Surveillance Plan
  • Post-Market Clinical Follow-up Plan

Legal Representative

When a Sponsor of a clinical investigation is not established in the European Union, the Sponsor should ensure that a Legal Representative is established in the EU. BeVinced can act as Legal Representative, herewith ensuring compliance of Sponsor obligations pursuant to the MDR. As Legal Representative, BeVinced will confirm the availability of required documentation and be the addressee for all communications with the Sponsor provided for in the MDR.


Based on many years of experience, we can assist in answering various challenges that manufacturers and users may face during the medical device lifecycle. Partner with us for a variety of consulting services, including but not limited to:

Quality Assurance and Compliance

Quality Management System implementation and review to comply with guidelines and regulations, such as MDR, ISO14155 and ISO13485.


Personnel training and qualification on various guidelines, laws, and regulations, including but not limited to MDR, ISO14155 and ISO13485.

Looking for a partner to place and keep safe, effective and affordable medical devices on the market?

Contact us