CDSCO INDIA

CDSCO INDIA

End-to-end regulatory approval — CDSCO, ICMR, NDHM, NABL. From docs to audits, we ensure full Indian compliance.

  • Test License (MD-13)
  • Import Test License (MD-17)
  • Clinical Investigation Permission (MD-23)
  • Manufacturing Licenses (MD-5 & MD-9)
  • Loan License (MD-10)
  • Import License (MD-15)
  • Wholesale License (MD-42)
  • Device Master File (DMF) construction
  • Plant Master File (PMF) construction
  • Risk Assessment of product (ISO 14971)
  • Usability Study (IEC 62366) assistance
  • Regulatory Risk Classification
  • Authorized Representative (AR) Service
  • MD online and NSWS account creation
  • Post Approval Change (PAC) submission
  • IEC 62304 (SDLC) documentation
  • MvPI (Materiovigilance program of India)
  • NPPA/DPCO communication and resolution
  • UCMPMD (Uniform Code for Marketing Practices in Medical Devices)
  • Free Sale Certificate (FSC)
  • Non-Conviction Certificate (NCC)
  • Market Standing Certificate (MSC)
  • NSQ (Not of Standard Quality) Resolution
  • FSCA (Field Safety Corrective Action) support