Service portfolio
ADD’s service portfolio covers all project development stages and enables clients to share synergies of a global alliance of pharmaceutical and engineering companies.
ADD has a long and successful track record in working with internationally operating pharmaceutical companies. Our committed team has succeeded in developing products for versatile applications including new chemical entities, line-extensions and generics.
• Elaboration of formulation and processing concepts
• Assessment of intellectual property rights
• Screening and selection of feasible prototypes
• Analytical characterization of raw materials,
intermediates and drug products
• Manufacturing of clinical trial material
• Optimization of selected product candidates
• Scale-up of a robust manufacturing process
• Technology transfer
• Regulatory services
• Commercial manufacturing
Development and manufacturing expertise
ADD combines strong scientific skills, expertise in developing complex formulations, pharmaceutical engineering and production capabilities to successfully bring your product to the market.
Integrated services
Your clinical trial material will be manufactured in our state-of-the-art cGMP compliant manufacturing sites located in Germany and in the USA. Our facilities are regularly inspected by our clients, local and international health authorities including the FDA. According to your needs we support scale-up and technology transfer activities to the selected commercial manufacturing site. Technology transfer activities could range from successful process validation and operator training up to turnkey engineering of new manufacturing facilities including installation of processing equipment. Alternatively we manufacture your products in our cGMP facilities for launch and commercialization.
With our skills, resources and systems we simplify the complex process
of launching and managing the lifecycle of your pharmaceutical product
with our international network.