Our expertise in FDA CFR 21 Part 11 ER/ES systems, providing regulatory compliant engineering, automation and validation solutions in pharmaceutical and healthcare industries. Our qualified engineers have an extensive technical and regulatory knowledge in generating protocols of VMP, IQ, OQ, PQ, SOP and can work with your staff in many areas to meet your validation and compliance needs as pertaining to data acquisition, Electronic Batch Record, Audit trail, Closed and Open systems.