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Skills

  • Client Development
  • Documentation Services
  • Medical Device
  • Regulatory Audits
  • Technical Documentation

Services

  • FDA 510(k) Submission- USA

    $50/hr Starting at $300 Ongoing

    Dedicated Resource

    I am an experienced Regulatory Affairs person. I have been working with Class1-3 manufacturer in this field. I have done multiple 510(k) submissions and successfully received the clearance for the clients...

    Client DevelopmentDocumentation ServicesMedical DeviceRegulatory AuditsTechnical Documentation