Delivering a successful sterile liquid dosage form from a finished API requires a high level of expertise and must address a wide range of issues - in a very demanding regulatory environment.
Development Services
Seeing the whole project - from the startAt IDT Biologika we offer the expertise and the critical personnel required for rapid, successful completion of the development phase of a liquid dosage form manufacturing project. Because we are familiar with the entire range of requirements of manufacture and registration of sterile liquid dosage forms, we can address issues before they become a problem - using an integrated prototype approach to the materials and methodologies we produce for you. With our development services, we employ some of the industry's leading scientists in formulation, process design and optimization as well as the creation and validation of analytical methods. |
Expert in the compilation of quality documentationWe offer a full-range of services for the clinical trials phase as well as stability tests, follow-up studies and optimization. Throughout our development activities, IDT Biologika is expert in the compilation of quality documentation for the establishment of application dossiers. At the end of the development process, we help you transition your project to full-scale manufacturing. At IDT Biologika, liquid dosage development means you will get the best product to market, faster with confidence in the regulatory phase. |
