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For over 30 years, IDT has provided a full scale service from initial API drug development to Clinical Trials. Globally, we’ve worked with 9 of the Top 10 Pharmaceutical companies, bringing a superior level of innovation and expertise to every project, whether cGMP high-potency API manufacture, finished dosage form development & scale-up, analytical testing, clinical packaging, or clinical trials and pharmacy services. Located in Melbourne and Adelaide, Australia our facilities are fully cGMP (GLP, GCP) and are audited by the US FDA and Australia’s TGA.
Having the right partner at every point of the development process is critical to your success. For over 30 years, IDT Australia has brought our expertise and innovation to projects large and small. Our culture is built on the importance of quality, and we take pride that we have worked with nine of the top ten pharmaceutical companies providing a flexible, full-scale service from early API and finished dose product development and clinical trial research through to commercial manufacture. Located in Melbourne and Adelaide we specialise in high containment, high potency manufacture of API and finished dose products (including beta lactams), analytical testing, clinical packaging and first time in man clinical trial research and pharmacy services. Our facilities are regularly audited by the US FDA and Australia’s TGA and operate to global quality standards.
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Successful companies rely on new products to keep them ahead of their competition. But conceiving, then developing drugs, and bringing them to market cost effectively needs knowledge, competence and a proven track record. For over 30 years, IDT’s range of skills, in-house capabilities and broad industry experience combine with proven processes and innovative management tools, to deliver tangible results.
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