Umedpharmalabs(UMPL) delivers state-of-the-art IT compliance solutions designed to meet the needs of today's rapidly evolving life sciences companies. As regulations and competitive pressures drive change, our consultants work closely with you to ensure that your company has the information infrastructure to stay current with regulatory requirements while leveraging the industry Best Practices for compliant IT systems.

We can assist you to align and optimize all aspects of your firms operations, from the CDS on the chemist's workbench, to the LIMS that manages your lab data, to the ERP that ties the lab to the rest of your organization. Whether you require a complete turn key implementation solution for a global multi-site project or a focused local deployment for a single site, our services can be scaled to your specific needs. For all our clients, our consulting services and products are designed to maximize your process efficiencies, improve your productivity and reduce your total cost of ownership (TCO).

Our life science professionals have worked in all areas of the drug discovery and approval process and have extensive backgrounds in management, IT, medicine and science. Our consultants are experts in the implementation, integration, and validation of leading commercial off the shelf software such as StarLIMS®, Documentum®, LiveLink®, Oracle Clinical™, Argus Safety™, TrackWise®, iRIS™, InForm™, RAVE™, Auditca™ and Audit Utopia™.

We work closely with you to leverage the abilities of your people, processes, and technology to maximize results. PSC's dedicated professionals understand all levels of the operation -- from management directives to laboratory processes -- and can help you to realize these needs in an integrated, holistic environment.

Our IT consulting services are specifically oriented towards servicing the needs of Manufacturing, Clinical and Research & Development (R&D). This includes refining and optimizing all computer and information technology systems, including: