We offer pharmaceutical firms full-service consultancy to make sure your operations follow the stringent Good Manufacturing Practices (GMP) guidelines. Our team of professionals is committed to assisting you in navigating Regulations, enhancing quality systems, and streamlining company procedures and practices to satisfy international compliance requirements. We provide a variety of consulting services that are customized to meet your unique requirements. Our staff is available to help you at every stage, whether you're trying to enhance your current GMP procedures or require assistance in regulatory compliance. Quality Management System (QMS) Development Regulatory Inspection Services Audit Services Training Services Validation Services Support for Preparation and Review of Documents (APQR, STP’s, Validations, Qualifications and et.) Supplier and Vendor Management Services Gap Analysis and Risk Assessment Services Documentation and SOP Development Services CSV as per GAMP5 and Audit trail Review for Data Integrity Product Lifecycle Support Services Investigations Improvement Services Regulatory Compliance Services Drug Master File (DMF) Services