Our GDP services include

• Gap Assessments based on EU GDP Guidelines, WHO GDP Standards, and US FDA regulations related to distribution, warehousing, and transportation of pharmaceutical products
• GDP Audits for wholesalers, distributors, logistics partners, and third-party logistics (3PL) providers
• SOP Review & Development covering storage, handling, packaging, and shipment processes
• Training Programs for GDP compliance, including temperature-sensitive logistics and documentation best practices
• Mock Inspections & Readiness Checks for upcoming regulatory audits by national or international authorities

GMP/ GDP/ GVP Compliance Auditor

• Offering regulatory experience ensuring full compliance with GMP/ GVP/ GDP standards, risk management, audits, product quality systems, CAPA management, deviation handling, and SOP documentation across clinical and post-marketing phases.
• Skilled in auditing manufacturing practices, deviation investigations, quality system maintenance, benefit-risk assessments, and audit follow-ups maintaining high standards of product quality and safety, managing regulatory compliance, and ensuring the integrity of the cold chain logistics.
• Direct oversight of import, distribution, storage, delivery, and post-market surveillance processes.
• Ensures alignment with GDP standards through quality agreements, site licenses, and product recalls.
• Oversight of documentation control and licenses for supply chain compliance, including import/export and storage practices.
• Involved in auditing and inspections and maintaining compliance with various regulatory frameworks.