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By your side from A to B
By your side from A to B
To receive expert support at any (or every) phase of the drug development lifecycle, reach out to book a consultation below.
To receive expert support at any (or every) phase of the drug development lifecycle, reach out to book a consultation below.
Share your details below
Share your details below
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WHERE WE HELP
The power of three, delivered globally
The power of three, delivered globally
We’ve navigated regulatory landscapes all over the globe, working with partners in the US, UK, Europe and Asia.
We’ve navigated regulatory landscapes all over the globe, working with partners in the US, UK, Europe and Asia.
FAQs
What you need to know with ABINITIO.
What is R&D?
R&D, or Research and Development, is the process through which scientific ideas are transformed into safe, effective, and innovative treatments. At ABINITIO, it means combining rigorous research, discovering how diseases work and identifying new therapeutic possibilities, with thoughtful development, where those discoveries are tested, refined, and brought closer to helping patients. It’s the vital engine that drives medical progress, where bright ideas become better medicines.
What is GMP?
GMP, or Good Manufacturing Practice, is all about making medicines with care, consistency, and integrity. It’s the strict set of quality standards that ensures every product is made safely, cleanly, and exactly as intended, from the first ingredient to the final package. Every dose we produce meets the highest standards of safety and reliability, so patients and healthcare professionals can have complete confidence in the treatments we deliver.
What are Clinical Trials?
Clinical trials are where things get real. They're carefully designed studies that help us understand whether a new treatment is safe, effective, and truly beneficial for human patients. They’re the bridge between scientific discovery and everyday medical care, where promising research meets real patients, under the close guidance of doctors, scientists, and ethics experts.
What’s the process for working with us?
Working with ABINITIO is simple, collaborative and tailored to you. We start by listening, understanding your goals, challenges, and the outcomes you want from it all. From there, we design a clear, step-by-step plan that brings together scientific insight, regulatory expertise, and open communication. You’ll always know where things stand, what’s next, and how we’re moving forward together. Whether you need us for all stages, or just one, we'll be right by your side, until you're out the other side.
Can I only work with you for one or two phases of development?
Absolutely. Our offering is end-to-end but modular, which means you can pick and choose which stage of the process you need us for. Whether you need us for one stage, two stages or all three stages, we can help.
What kind of dosage forms can you help me with?
We can help with a wide range of complex dosage forms, including Topical, Oral, Nasal, Injectables, Opthalmic and Respiratory, to name but a few.
How quickly can you get me to trial?
We can get you from bench to clinic in 18 months. Our integrated process results in a faster process, because you don't have to use multiple suppliers and there's less handover friction at each stage.
Am I eligible for a tax incentive?
Yes. ABINITIO is a registered RTGI service provider, so all three phases of the process count as research under the Australian Government's tax incentive schemes.