Vgmpsolv

Comprehensive Pharma Quality Audits, Contract & Compliance Services We provide end-to-end Quality, Compliance, and Regulatory support to help global pharmaceutical, healthcare and life-science companies achieve GxP excellence, audit readiness, and operational efficiency. Quality Audits & Compliance Conducting third-party GxP audits, vendor/supplier audits, and external audits aligned with international regulatory standards. Ensuring any-time readiness for regulatory inspections and customer audits. Investigations & CAPA Investigation of OOS, OOT, OOE, OOC, deviations, market complaints, lab incidents, returns, and data integrity issues. Identifying true root cause and implementing effective, sustainable CAPA. Regulatory Documentation & Filings Compilation and submission of regulatory filings as per global requirements. Preparation and review of SMF, VMP, SOPs, protocols, and Quality Plans. Responsible for preparation of all GxP documents. QMS Implementation & Continuous Improvement Implementation of QMS, cGMP systems at both site and corporate levels. Effective implementation of Change Control, QbD, 5S, Kaizen, Cpk, Six Sigma, PLM, FMEA, FMECA, and risk-management systems. Validation & Qualification Services Conducting process, cleaning, transport, and equipment validations. Preparation and review of URS, DS, DQ, FS, RA, IQ, OQ, PQ. Supporting route scouting and new product launches with R&D/ARD teams. Quality & Technical Documentation Preparation and review of Quality Risk Assessments, Impact Assessments, and Quality Metrics. Review of QC/Micro data, SOPs, STPs, BCRs, BPCRs. Training & Capability Building Conducting internal and external trainings using effective learning methodologies for all pharma functions. Cost Optimization & Process Improvement Implementation of cost-saving and cost-reduction initiatives, improving process efficiency and reducing operational burden. Elevate your GMP with expert Supplier audits