NADRACT is a well-regarded pharmaceutical, consumer goods and medical devices Regulatory Affairs Company that has been operating in Australia for over 10 years regulatory affairs experience. At NADRACT, we are expert in combining the parallel requirements of pharmaceutical, neutraceuticals and therapeutics industry.

NADRACT understands the importance of over-the counter medicines, complementary medicines, prescription medicines, veterinary medicines, consumer goods, cosmetics and medical devices and have confidence in supplying the Australian market with quality products. We are proud to work alongside the best and reputed team to deliver high quality solutions.

Consumer goods and medical devices Regulatory Affairs is both a legal requirement and good business practice. Our experienced regulatory affairs consultant will be taking care to provide the best GMP, submission, TGA, Prescription, OTC, Complementary medicines, Medical Devices, Variation, Dossier applications, CPP and Export applications. We have strong pharmaceutical, consumer goods and medical devices networks, an in-depth knowledge of regulatory requirements, and a sound working relationship with Regulatory Affairs consulting company.

Our professional and experienced complementary medicines Consultant Australia have the ability to provide practical and cost effective solutions. NADRACT provides efficient services to help safeguard quality and ensure the maintenance of registrations in Australia.

Our professional and experienced regulatory affairs consultant specialise in the Australian Therapeutic Goods Administration (TGA) and New Zealand Medsafe requirements and will assist you to meet specific medical devices Regulatory requirements.

Contact us for non-obligation quote on +61 (0) 3 831 34832 and we will put you in contact with one of our experienced regulatory affairs consultant.