CRO Services in Medical Device’s Clinical Trial
MED DEVICES is a Contract Research Organization and a pioneer in providing the entire spectrum of clinical research services exclusively for medical devices
We have extensive experience of conformity assessment and understanding of Medical Devices as per European Directive MDD 93/42/EEC, IVDD 98/79/EC, AIMD 90/385/EEC and USFDA.
MED DEVICES focus area in healthcare is Clinical Trial Management & Execution, Site/ Project Management, Monitoring Services, Data Management & Medical/ Report Writing, Training & Development, Regulatory Services. MED DEVICES could be a partner to your organization either for a single service or for the full range of our professional services customized to individual needs.
MED DEVICES can help your company to successfully plan and complete clinical investigations to assess device performance and safety in compliance with ISO 14155 standards and ICG- GCP requirements. We have a team within the operations that provides exclusive support in conducting Device Trials in different therapeutic areas.
MED DEVICES provides superior Clinical Research Support services to medical device industry. Our solutions are designed to address the bottlenecks in the area by
- Reducing costs using innovative outsourcing models
- Improve operational efficiencies
We are dealing in following therapeutic areas-
- Orthopaedics
- Cardiology
- Vascular Surgery
- Respiratory
- Ophthalmology
- Dermatology
- Gastroenterology
- Plastic Surgery
- Spinal
Our Strengths includes Service Excellence, Total Quality Management, GCP adherence and compliance, Unparalleled value for money, Young and motivated team, Thorough understanding of regulatory policies & processes (local & global)
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