US-PHARMASERVE INC. is an outsourcing, program management and consulting group specializing in research, process design & development, pre-clinical work up, and the cGMP production of biologics for the Phases I & II clinical trials, as well as ISO-9001 manufacturing of diagnostic reagents and kits. We have significant in-house expertise and ready access to an impressive network of over 300 world-class subject matter experts, freelance consultants, sub-contractor, vendors and service providers to outsource and manage your projects. Our business model encourages and fosters participatory decision making by our clients. Our Mission: To custom design and execute the best-in-class outsourcing solutions for our clients so that their programs and products are completed and delivered: On their timeline,within their budget,meeting their final product specifications with the quality they expect Achieving compliance with cGMP, ISO, or other regulatory guidelines' We outsource and manage your projects in the following areas: Process Design, Development, R&D and Preclinical Work-up cGMP Clinical Trials Material Manufacturing and sterile liquid fill finish Formulation development and Stability Studies Safety Studies . Marketability studies. Management consultation (due diligence, valuation, strategy, restructuring, and financial transactions), scouting for seed and early stage venture funding. Medical and technical writing and editorials