Medical Writing

Our collaborative and astute team of medical writers can support you in all stages of your clinical trial, from protocols, clinical investigation plans (CIPs) and study designs to final clinical study reports. With our expertise, data-driven approach and breadth of experience, you can be assured that all your medical writing will be completed to the highest possible standard, setting up your clinical trial and product for future success.

Clinical trial protocol writing

As a CRO early phase specialist, our medical writers are well-equipped for clinical trial protocol writing and review, from First in Human to Phase 3 and beyond. With in-depth knowledge of treatment practices and standards of care, we are experts at writing protocols and CIPs that balance scientific evaluation with on-site practicality, investigator engagement and subject recruitment considerations. We also have established relationships with many therapeutic area leaders who can provide their expert opinion prior to finalisation of your protocol or CIP.

We can assist with:

Clinical trial protocol writing
Clinical study report writing

Clinical study report writing

Clinical study reports are key to the commercial viability of your product. Our medical writers, in collaboration with our team of expert biostatisticians, can present the results, analysis and interpretation of your study accurately, clearly and concisely, while also guaranteeing that your report meets the content and format requirements of international regulators.

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Phase 1 study, local Biotech company

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CEO, Australian Medical Device Company

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