Redwood Pharma Consulting offers a comprehensive and distinctive quality service to the pharmaceutical industry based on more than 40 years of experience in QA, Production and Technical functions.
Expertise and support are specifically in Qualified Person capability (MIA and IMP), quality audits (API and secondary manufacturing operations), EU GMP Gap Analysis and MHRA/FDA inspection preparation. Additional guidance and training can be provided in GMP training (multiple topics), reviewing the effectiveness of Quality Risk Management and Quality Management Systems and identifying improvements in Root Cause Investigation and CAPA.
Client lists (current and historical) are available on request, together with any references required.
GMP compliance and risk-based audits of product quality and the supply chain all have their place in assessing controls.... Read More
Redwood Pharma Consulting has proven experience in the application and assessment of Quality Risk Management (QRM)... Read More
Redwood Pharma Consulting recognises the importance of a structured approach to conducting Root Cause Investigations... Read More