Navigating the complex and continually evolving landscape of regulatory expectations is a primary challenge for pharmaceutical manufacturers. PGF Pharma International provides expert GMP consultancy to help you develop, implement, or enhance your Quality Management System (QMS).

We focus on aligning your QMS seamlessly with both stringent EU-GMP requirements and your internal business strategies and operational processes, paving the way for regulatory success. Our services are designed to facilitate effective GMP implementation or upgrades and support you in securing essential manufacturing certifications and licenses.

Our Core GMP Consultancy Services Include:

• Strategic GMP Consultation: Tailored advice on GMP compliance strategies.
• Mock Inspections & Audit Readiness: Simulating regulatory audits to identify gaps and prepare your team.
• On-Site GMP/cGMP Consultations: Hands-on support and assessment at your facilities.
• Quality System Design & Optimization: Developing or refining robust and compliant quality systems.
• Comprehensive Documentation Review: Ensuring your SOPs and records meet GMP standards.
• Laboratory Practice Implementation: Establishing compliant laboratory controls and practices (e.g., GLP aspects within GMP).

End-to-End Inspection & Project Support:

• Beyond core consultancy, we offer comprehensive support throughout the regulatory lifecycle:
• Inspection Preparation: Guiding your team through readiness activities for Health Authority inspections.
• Findings Management: Assisting in addressing inspection findings and formulating effective responses.
• License Application Support: Compiling and reviewing documentation for manufacturing license applications.
• Health Authority Liaison: Facilitating communication and arrangements for official GMP inspections.
• Targeted Business Support: Providing specialized assistance for specific GMP-related projects or challenges.