NADRACT provides end-to-end regulatory affairs services throughout Australia. Our experience covers all types of over-the counter medicines, complementary medicines, prescription medicines, veterinary medicines, consumer goods, cosmetics and medical devices.

Our highly-respected and experienced regulatory affairs consultant has decades of experience in delivering regulatory solutions and strategic guidance. We have been tackling some of the most technically challenging projects, delivering successful client outcomes that are flexible and cost-effective and that offer exceptional value to clients. We deliver projects that are flexible and scalable in nature, helping our clients with registration and maintenance of registrations of veterinary medicines, consumer goods, cosmetics and medical devices.

We take pride in the excellent reputation we have built for delivering regulatory affairs services including Dossier submission, Variation applications, Gap-analysis reports, Regulatory support throughout the life-cycle of product, Declaration/Maintenance of product annual charges, PBS applications, TGA GMP clearance and Representation of overseas.

NADRACT understands that every project is unique. As a result, NADRACT offers a flexible approach to achieve client’s objectives. Our highly-respected and experienced regulatory affairs consultants work closely with companies for registration of medical devices, maintenance of product registrations, liaise with the TGA &/or Medsafe and regulatory enquiries.

For more information on registration and maintenance of registrations of veterinary medicines, consumer goods, cosmetics and medical devices, please contact us and we will respond to you as soon as possible.