Valoit is a premier provider of FDA and SOX regulatory compliance services to companies in the finished pharmaceutical, bulk pharmaceutical, biotechnology, medical device, and medical diagnostic industries. Our expertise in these core areas enables us to provide audit, assessments, validation, and quality assurance services to address the challenges faced by life science companies.

Our core competency in engineering design, information technology, process controls and knowledge of cGXPs differentiates us from our competitors and offers our clients a reliable source to meet all their technology and regulatory compliance needs. Valoit professionals are skilled at creative thinking, analytical problem solving and detailed execution.

Valoit provides its clients with a total solution for regulatory compliance including validation and quality assurance on projects. The use of computer systems and automation has become common place in pharmaceutical applications. We provide validation for very sophisticated computer controls to basic levels of automation. These include SAP, ERP, MRP, MES, PLCs, DCS, SCADA, Laboratory Information Management Systems (LIMS), Electronic Document Management Systems (EDMS) and other enterprise and automated systems. We provide equipment, facilities, and utilities validation also.