The Global Medical Affairs & Medical Writing Consultancy

Regulatory / Quality Compliance Consulting

Pharmaceutical and Medical Device

To further support our valued customers, we provide consulting services in the areas of Regulatory Affairs & Quality Compliance.

Global Regulatory Affairs / Quality Compliance Consulting Services:

  • Clinical Trial Set-Up
  • CTC Registrations & Disclosures
  • CRO Management & Solutions
  • Marketing authorization / License Renewals
  • NDAs / Variations / Amendment Filings
  • Global GMP Mock Audits
  • Global Manufacturing Authorization
  • Global Regulatory Management
  • Global Labelling / Packaging Requirements
  • Global Regulatory Agency Interfacing
  • Guarantee a Hassle-Free Market Approval

Want to know more?
We’re just scratching the surface. Contact us by phone or email, and let’s see how our team can interface with yours. We look forward to hearing from you .