our company

IDT specialises in the development, scale-up and production of active pharmaceutical ingredients to international standards of Good Manufacturing Practice (cGMP). IDT has over 25 years experience in the handling of :

• Cytotoxic Active Pharmaceutical Ingredients (API's)
• High Potency API's
• Hormones
• Toxic Reagents

IDT manufactures Active Pharmaceutical Ingredients (API's) for world-wide clients in its FDA inspected containment facilities located in Melbourne Australia.

IDT also specialises in the entire post-discovery pharmaceutical life cycle. Our expertise in the development of new chemical entities from laboratory-scale to full-scale production, combined with our ability to conduct Phase I-II clinical trials, uniquely positions IDT to assist companies at many stages from synthesis to market