Our Services  
  
   
Third party inspection
CE | USFDA
Vendor Sourcing
Clinical Investigation
  • Clinical Trial Management & Execution
  • Site/ Project Management
  • Data Management
  • Regulatory Professional Certifications
    Representation Services
  • European Authorized Representative
  • Only Representative (Reach     2006/1907)-
  • Marketing Services
    Stability Studies

     

    At MED DEVICES , we measure our success by the success of your project. We work as an extension of your organization, a strategic partner to complement your team. Empowered by a dedicated team of well experienced CRA's, CRC's and other professionals, our project manager act as single point of contact in ensuring successful completion of your project. Each member of our project team is experienced enough to Put Right Ingredients of Success to your project.

    MED DEVICES Whether a single service or complete management package, choose MED DEVICES to deliver you with a professional service of the highest quality.

    Services-
    - Feasibility Assessment & Project Milestones Planning
    - Investigator Site Evaluation & Selection
    - Development of Essential Trial Documents (Protocol, ICD & CRF)
    - Translation & Validation of ICD in Local Languages
    - Coordination for Ethics Committee & Regulatory Approvals, Study Initiation
    - Quality Control & Quality Assurance

    Independent Auditing
    - Process Audits (Sponsors, CROs)
    - Compliance Audits (CROs, Investigator Sites)

    Medical Writing
    Preparation of Study Reports, Manuscripts, Posters, Abstracts etc.

    You can reach us by Mailing us at info@meddevices.net

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