Regulatory affairs are responsible of obtaining approval for new pharmaceutical products and ensuring its benefits in the medical fields. In order to protect the safety of food and medical products, it is crucial to keep all the procedures clean with any biased information and ill practices.

NADRACT have been engaged in Regulatory Affairs Consultant and Complementary medicines Consultant in Australia. With us, getting phenomenal services of Regulatory Affairs, Consultant, GMP, submission, TGA, Prescription, OTC, Complementary medicines, Medical Devices, Variation, Dossier applications, CPP, Export applications, and more is no more a trouble for anyone.

We are a company of highly experience and skilled consultants that has more than 10 years regulatory affairs experience in the field. Our clients based on small, medium and large pharmaceutical companies, to which we provide our much satisfactory services of pharmaceutical, veterinary medicines, consumer goods and medical devices Regulatory Affairs.

NADRACT offers professional environment, flexibility, high quality, and solutions to all of our client’s problems and requirements. With our experienced Regulatory Affairs Consultant, we tend to support all the projects from the initiative process until the end of the product cycle.

To connect with any of our consultant for detailed information of our services you can send an email at [email protected] or you can also contact us by calling at +61 (0) 3 831 34832.