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Operon Strategist
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    • TURNKEY PROJECT CONSULTANTS
      • PRODUCT FEASIBILITY & DETAIL PROJECT REPORT
      • MANUFACTURING FACILITY
      • VALIDATION DOCUMENTATION
      • CLEAN ROOM GUIDANCE
      • MDSAP – Medical Device Single Audit Program
      • QUALITY MANAGEMENT SYSTEM
        • FDA 21 CFR PART 820 QUALITY SYSTEM REGULATION
        • ISO 13485 – QMS MEDICAL DEVICE
        • ISO 15378 CERTIFICATION | PRIMARY PACKAGING REGULATORY CONSULTING
    • REGULATORY APPROVALS
      • ANVISA Medical Device Registration in Brazil
      • FDA 510(K)
      • CDSCO Registration for Medical Devices
      • CE Marking
      • Medical Device Registration in Saudi Arabia (SFDA Approval)
      • Medical Device UKCA Certification Services for Brazil Manufacturers
    • Medical Device Design and Development Services
      • Drug Device Combination Product Consultant in Brazil
      • US FDA 21 CFR 820.30 DESIGN CONTROL REQUIREMENTS
  • TESTIMONIALS
  • BLOG
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Email
logo-operon-website
Operon Strategist
  • Home
  • Services
  • Regulatory Approvals
  • About Us
  • BLOG
  • Contact Us
  • Home
  • Services
    • Medical Device Turnkey Project Consultants
      • CLEAN ROOM GUIDANCE
      • FDA 21 CFR PART 820 QUALITY SYSTEM REGULATION
      • ISO 13485 – QMS MEDICAL DEVICE
      • ISO 15378 CERTIFICATION | PRIMARY PACKAGING REGULATORY CONSULTING
      • MANUFACTURING FACILITY
      • MDSAP
      • PRODUCT FEASIBILITY & DETAIL PROJECT REPORT
      • QUALITY MANAGEMENT SYSTEM
      • VALIDATION DOCUMENTATION
    • Regulatory Approvals
      • ANVISA Medical Device Registration in Brazil
      • CDSCO Registration for Medical Devices
      • CE Marking
      • FDA 510(K)
      • Medical Device Design and Development Services
        • Drug Device Combination Product Consultant in Brazil
        • US FDA 21 CFR 820.30 DESIGN CONTROL REQUIREMENTS
      • Medical Device Registration in Saudi Arabia (SFDA Approval)
      • Medical Device UKCA Certification Services for Brazil Manufacturers
  • TESTIMONIALS

Operon Strategist is a medical device regulatory consulting company that provides regulatory advice and guidance to various manufacturers in Brazil to ensure the strategic development of these manufacturers.

Services

  • Regulatory Approvals
  • ANVISA Registration
    • FDA 510(K)
    • CDSCO Registration
    • CE Marking
  • Turnkey Project Consultants
    • Clean Room Guidance
    • Manufacturing Facility
    • Quality Management System
  • More Services

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Mail Us: enquiry@operonstrategist.com