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Drug and Device Development

Drug and Device Development | Working with your CDMO and CMOs, management of outsourced testing and non-clinical studies. Facilitation of technology transfer and writing / review of technical protocols and reports.

Adjutor Healthcare

Adjutor Healthcare partners with businesses to bring new medicines and medical devices to market. We focus on regulatory strategy, product registration/ lifecycle management, quality/QMS, market access, distribution and commercialisation so your innovation can reach the people who need it most.

At Adjutor Healthcare, we specialise in bridging the gap between innovation and impact. From navigating complex regulatory requirements to developing market access and commercialisation strategies, we work with you to ensure your medicines and medical devices reach the people who need them.

We are specialists in drug and device development requirements.

How our highly skilled team can help you –

Working with your CDMO

Working with your CMOs

Management of outsourced testing

Management of non-clinical studies

Facilitation of technology transfer

Writing and review of technical protocols and reports

Data management and biostatistics

Medical writing

ICH, ISO and local requirements

The secret of getting ahead is getting started.

Mark Twain

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.

Let’s talk