Areas Served

In Australia, the Therapeutic Goods Administration oversees the regulation of medical devices. This means that before a medical device can be sold in Australia, it has to be listed on the Australian Register of Therapeutic Goods.

If you are a medical device manufacturer and need help with TGA submissions and registration, Vicki Partridge has extensive experience both within the TGA, and as an external consultant representing medical device manufacturers around the world and gaing inclusion of their products on the ARTG.

The medical device industry in Asia is known to be challenging due to the complicated changes in the regulatory demands and market dynamics. To penetrate this market and keep up with the changing regulations, an experienced medical equipment consultant is needed. Vicki Partridge has extensive experience in this area.

Backed by years of experience in the medical device regulatory industry, Vicki Partridge can help you in every aspect of your medical device business.

The medical device industrry in Europe is underegoing extensive change as the new Medical Device Regulations come into play. Vickin Partridge represents manufacturers all through Europe and provides valuable guidanvce as they as they adjust to the new requirements.

Vicki Partridge has an extensive client list throughout the United States, including three companies capitalised in excess of US$1 Billion. Vicki has assisted these companies to gain regulatory approval to sell their products into the US, Asia, Europen and Australian markets.​

We take care of all of your MEDICAL DEVICE REGULATORY CONSULTING SERVICES needs.