Clinical studies are the essential step in ensuring your product is safe and effective, and that it fulfills its intended use. Fervor offers clinical solutions for today’s dynamic medical device and diagnostics industry.
Combined with experience and expertise for providing best quality and cost effective time bound solutions, we ensure you stay on time and on budget for your pre-market to post-market product lifecycle.
Development for medical technologies can be challenging without the right people, processes, evidence and insights
What can we offer?
What can we offer?
With decades of experience conducting medical device clinical studies to European requirements. We offer a turnkey CRO solution and manage end to end post-market medical device clinical studies.
Fervor global clinical experts:
Bespeak Proof of Principle or First in Man (FIM) studies.
Demonstrate Clinical safety and performance /effectiveness for CE Marking.
Procure post-market clinical evidence data with CE Marking.
Conduct HEOR and derive to generate scientific evidences.
Generates clinical evidence for marketing claims
Right from preparation of your clinical study strategy to completion of study report, we manage every aspect in compliance with all applicable quality aspects.
Integrity is the key for our deliverables.
Medical Device Clinical Trial Inception and Management
How we do:
Project management
Study start up activities including Investigator and site selection/recruitment
Clinical Writing including Study design input/review - optimization of endpoints
Vendor identification, control and management (e.g., central lab etc.)
Clinical Study insurance support
Competent Authority and Ethics Committee submission and liaison.
Regulatory Compliance management
Study monitoring
Data management services
Clinical writing (Protocol, CSR, CER, study related documents and tools etc.)