Global Healthcare Development and Commercialisation
Specialists in end-to-end development and commercialisation of medicines and medical devices.
Your first choice for expert services!
Our Specialist Services
No matter what your stage of product development or marketing, we can provide an experienced, tailored team to support your business objectives.
Why Choose Adjutor Healthcare
Of the many partners to choose from, it can be hard to find one you can rely on and build a relationship with. Here are 4 reasons why you’ve made the right decision in choosing us.
Our Management Team
Our Latest News
Stay up to date with industry developments in Australia/New Zealand and beyond.
Is Artificial Intelligence Becoming Too Smart for Regulators? AI is Everywhere and it isn’t that New! The term ‘artificial intelligence’ (AI) was first coined in the 1950s. Since then, this disruptive idea has come a long…
The long-awaited transition to the EU Medical Devices Regulation (MDR) is looming. The regulatory realm of medical devices is in a state of flux and poised on the brink of the most significant change to the…
Australian science and technology sectors are talking about a ‘research revival’ as the Federal Government splashes the cash in the 2020 Budget. 2020 Budget Cash Splash Thanks to COVID-19, early October saw the first Australian federal…
By now, we should all be very familiar with the new Form for providing Product Information (PI) for Australia. Each time you make a change to a PI, be it safety-related or otherwise, you’re required to…
We may have a global market but do we really consider options outside of USA and EU when developing our Therapeutic Product Commercialization strategy? The USA, EU/UK are large markets with clear regulatory requirements, so they…
Since 2015, Medsafe NZ, the New Zealand Medicines and Medical Devices Safety Authority, has been working on a new therapeutic products regulatory regime to replace and modernise the regulatory arrangements for medicines, and provide regulation of…
Our Success Stories
“I highly recommend Rosalie’s team and their support for regulatory filings. They are extremely knowledgeable and integrate easily with US based companies to execute filings in AU/NZ. I have worked with Rosalie at more than 1 company and would absolutely hire them again in the future.”
– Heather Tokatlyan
Senior Director Regulatory Affairs at Deciphera Pharmaceuticals
“We have been working with Adjutor for over 3 years and have always found Adjutor staff to be friendly, professional, committed and extremely knowledgeable in their field. Their unwavering focus and commitment to our projects, often with tight deadlines, has earned the respect and loyalty of our organization. It is a pleasure working with Adjutor and I would highly recommend their services to any organisation seeking an experienced and approachable regulatory team.”
– Maria Rundell
General Manager Landauer Radiopharmaceuticals
“I give my highest recommendation for Rosalie. She has broad experience in product development for drugs and devices, including expertise with clinical and regulatory strategies, protocol design & operational details, and medical & regulatory writing. She is a very creative thinker. I would gladly take her on my team!”
– William (Bill) Sietsema
Vice President, Global Regulatory Affairs at Caladrius Biosciences