Adjutor Healthcare is a leading healthcare services company operating globally.
No matter what your stage of product development or lifecycle, we can provide an experienced, tailored team to support your business objectives.
Strategy and Project Management
Strategy is key to everything we do. We will design a focused plan of how to achieve your commercial product vision.
Development and Clinical
We are specialists in drug and device development requirements, including lab, non-clinical and clinical, as well as acting as a CRO.
Regulatory Affairs and Market Access
Adjutor are experts in regulatory affairs and market access, able to guide you to market efficiently and effectively.
Sponsorship and Commercialisation
We can help you to access a wide variety of countries and ensure effective commercialisation and product launch strategies.
Quality and Training
We provide QMS system design & implementation that is fit for your purposes, training of staff in the QMS together with a variety of auditing solutions.
Risk Management
RMP development, writing and review of technical protocols and reports.
Registration Pathways
Orbis / ACCESS / Orphan / Provisional / Priority and other expedited pathways.
QMS System Design
Comprehensive audits covering GMP / GLP / GCP / GDP / ISO9001 / ISO13485.
Data Analytics
Understanding and managing your data and biostatics.
Why Choose Us?
We get SMEs and the Adjutor Advantage is how we demonstrate, every day, that we are a great partner for your business. We’re engaged, and motivated, to help you at each stage of your journey to market and beyond.
Our Responsiveness
Quick to respond with an appreciation of your commercial drivers.
Our Drive & Agility
Our exceptional drive and agility allows us to expedite your projects.
Our Flexibility
Understanding and adapting to your evolving needs.
Our Experience & Expertise
Our team has extensive industry experience and are multi-skilled.
Our Collaboration
We work seamlessly as an extension of your team.
Our Reliability & Quality
Effectively delivering high quality services.
Learn More About Us
We’re a company of down to earth, like-minded, individuals who are enthusiastic and engaged, with a love of life and learning. We work in a collegial way to support each other and our clients.
Latest Insights
Insights • Articles • Latest News • Regulatory Announcements
Stay up to date with industry developments in Australia/New Zealand and beyond.
Understanding TGA GMP Clearance
Understanding TGA Good Manufacturing Practice (GMP) requirements for Australian Regulatory Submissions Good Manufacturing Practice (GMP) is vital in ensuring the quality, safety, and efficacy of the therapeutic goods for human use (including sunscreens). In Australia, the Therapeutic Goods Administration (TGA) oversees the implementation and enforcement of GMP standards to uphold the integrity of the pharmaceutical…
Choosing the Right Regulatory Affairs Consultant
Whether you are part of an established team, a start-up, an SME, or a founder, navigating the stringent requirements of the Medical Technology, Biotechnology, and Pharmaceutical (MTP) sectors can be complex and challenging. This is where partnering with the right Regulatory Affairs Consultant becomes invaluable. Understanding the Role of a Regulatory Affairs Consultant A regulatory…
Cell and Gene Therapies Regulation
Navigating the Regulation of Cell and Gene Therapies in Australia and New Zealand Globally, cell and gene therapies are revolutionising modern medicine, offering groundbreaking treatments for life-threatening conditions including cancer, genetic disorders and rare diseases. However, despite the pace of scientific innovation, regulatory frameworks in many countries, including Australia and New Zealand, have struggled to…
Ready for growth?
Contact us today and let’s work together to achieve your goals. Whether you have a question, need more information, or want to discuss your project, our team is here to help.