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Mittal Consulting's V&V Review ensures compliance for medical device companies:

  • Documentation Review:
    Thoroughly examining key documents.
  • Regulatory Compliance Assessment:
    Aligning with 21 CFR Part 820 and 21 CFR Part 807.
  • Verification and Validation Review:
    Assessing critical processes for effectiveness.
  • Risk Assessment:
    Identifying potential device-related risks.
  • Data Analysis:
    Analyzing relevant data comprehensively.
  • Compliance Gap Identification:
    Spotting and addressing compliance gaps.
  • Quality System Integration:
    Ensuring seamless integration within the quality system.

With Mittal Consulting, your medical device undergoes a concise V&V Review, meeting regulatory standards for safety and efficacy.