As the largest healthcare contract manufacturer in the Asia-Pacific region, GMP has teams based locally in our Auckland, Sydney and Beijing offices, who are able to give expert advice on a broad range of requirements including those issued by Medsafe, TGA and SAC. Through our highly qualified Regulatory Affairs teams, we offer our clients expert consultation over the full scope of regulatory compliance.

  • Regulatory compliance with Medsafe and MPI
  • Expertise in regulatory compliance with Chinese GB standards
  • Label compliance
  • Preparation of Registration Dossier for international markets
  • Export certification
  • Import permits
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