GMP Pharmaceuticals

Regulatory

As the largest healthcare contract manufacturer in the Asia-Pacific region, GMP has teams based locally in our Sydney, Auckland and Beijing offices, who are able to give expert advice on a broad range of requirements including those issued by TGA, Medsafe 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 TGA and FSANZ
• Expertise in regulatory compliance with Chinese GB standards
• Label compliance
• Preparation of Registration Dossier for international markets
• Export certification
• Import permits