The
Adjutor Group

The Adjutor Group 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.

Regulatory Affairs and Market Access | TGA Regulatory Affairs Consultants Australia: Adjutor are experts in regulatory affairs and market access, able to guide you to market efficiently and effectively.
Sponsorship and Commercialisation | Adjutor can help you to you access a wide variety of countries and ensure effective commercialisation and product launch strategies. North and Latin America, Europe/UK, Asia/Pacific, Middle East.
Quality and Training | Whether your existing quality system needs a refresh or you’re just embarking on your first quality journey, Adjutor can help with documentation, training and auditing.

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.

Adjutor Healthcare Strategy and Project Management | Strategy is key to everything we do! Development, regulatory, commercialisation, and market access strategy. Integrated project plans and ongoing project management.

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.

Adjutor Healthcare are specialists in drug and device development requirements, including lab, non-clinical and clinical, as well as acting as a CRO.

Drug and Device Development

We are specialists in drug and device development requirements, including lab, non-clinical and clinical, as well as acting as a CRO.

Adjutor Clinical provides comprehensive clinical trial services for medicines, medical devices and cell and gene therapies, to smooth your path to product approvals globally.

Clinical Trial Services

Adjutor Clinical provides comprehensive clinical trial services for medicines, medical devices and cell and gene therapies.

Adjutor handle all aspects of clinical trial preparation, from planning and protocol development to securing permits and ensuring regulatory readiness, so your studies start on the right track.
The Adjutor clinical trial operations team ensures your studies run smoothly from start to finish. We manage site setup, monitoring, logistics, and compliance, keeping your trials on track and delivering high-quality data.

Risk Management

Registration Pathways

QMS System Design

Data Analytics

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.

Learn More About Us

Latest Insights

  • Pharmaceutical Quality Assurance Australia and NZ

    Pharmaceutical Quality Assurance Australia and NZ

    The Critical Importance of Quality Assurance (QA) in Drug Development, Clinical Trials, and Importation into Australia and New Zealand. Why Pharmaceutical Quality Assurance Matters Maintaining high-quality standards throughout every stage of drug development, including nonclinical research, clinical trials, manufacturing, supply chain, and importation, is essential for protecting patient safety, ensuring product efficacy, and fulfilling regulatory…

  • Australia and the ACCESS Consortium: Navigating Regulatory Collaboration

    Australia and the ACCESS Consortium: Navigating Regulatory Collaboration

    The Access Consortium is a coalition of like-minded regulatory authorities working together to promote greater regulatory collaboration and alignment of regulatory requirements. Learn how the ACCESS Consortium can streamline medicine approvals in Australia and partner countries, accelerating access to new therapies. Australia as an Early Entry Market for Medicines Australia is an increasingly attractive early…

  • Life Sciences Expansion Strategies Greater Bay Area – China

    Life Sciences Expansion Strategies Greater Bay Area – China

    China’s Greater Bay Area (GBA) initiative aims to create a single, integrated economic zone, fostering innovation, connectivity, and environmental sustainability. We explore how the Greater Bay Area (GBA) is transforming life sciences and medical device access in China, with regulatory benefits and streamlined market entry opportunities. What is the Greater Bay Area (GBA)? The Greater…

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.