Quality Support for Manufacturing Services

Manufacturing excellence depends on more than compliant processes. It requires experienced quality professionals who can strengthen your quality systems, support regulatory expectations, and ensure uninterrupted product release across increasingly complex global supply chains.

PLG provides flexible Quality Support for Manufacturing Services, combining Qualified Person (QP), Responsible Person (RP), GMP, and Quality Management expertise to help pharmaceutical and biotechnology companies maintain compliance while ensuring operational continuity. Whether you need interim quality leadership, support after regulatory inspections, or assistance in obtaining manufacturing licences, our specialists integrate seamlessly with your teams to deliver practical, risk-based solutions.

• Qualified Person (QP) certification and batch release services for human and veterinary medicinal products across the UK and EEA

• Interim Contract Qualified Person (QP), Responsible Person (RP), and Responsible Person for Import (RPI) services

• Wholesale Distribution Authorisation (WDA) application, Responsible Person (RP) support, and ongoing licence management
• GDP compliance consulting, warehouse operations support, and distribution quality management expertise
• GMP compliance consulting and Manufacturing & Import Authorisation (MIA) application support
• Quality Management System (QMS) development, gap assessments, and continuous improvement
• Manufacturing licence preparation and regulatory readiness
• Inspection remediation and CAPA implementation following MHRA, EMA, FDA, or other regulatory findings
• Supplier qualification, GMP audits, and contract manufacturing oversight
• API qualification and certification support
• Importation, storage, distribution, quality control testing, and batch release oversight
• Manufacturing, packaging, and testing site audits
• Quality support across solid, liquid, sterile, topical, and inhalation products

• Maintain uninterrupted product supply through reliable QP certification and batch release

• Strengthen GMP and GDP compliance with practical, inspection-ready quality systems

• Accelerate MIA and WDA approvals through expert regulatory support

• Reduce compliance risk with experienced remediation and quality oversight

• Scale quality resources quickly through flexible interim QP, RP & RPI support

• Protect patient safety while ensuring operational efficiency across the manufacturing, storage and distribution activities

Whether you require interim Qualified Person support, Responsible Person services, remediation support following a regulatory inspection, or strategic guidance to strengthen your manufacturing quality systems, PLG provides the expertise to help you maintain compliance, protect supply continuity, and confidently meet regulatory expectations.