GMP Foundation specializes in the design, assessment and improvement of GMP and Quality Management Systems in pharmaceutical manufacturing and consumer healthcare Industries. Our Experts have more than decades of experience in the development of effective GMP and quality assurance procedures, auditing of manufacturing facilities, provision of GMP training courses and detailed preparations for regulatory inspections. We have in-depth experience to carry out Validation (Process /cleaning/methods) and Qualification activities particularly for bulk intermediates, APIs and Dosage forms.Our Chief consultant is an experienced international auditor of suppliers and contractors and has successfully prepared several sites for regulatory inspections (FDA/MHRA/TGA/WHO-GMP). He is an international consultant in cGMP training and design/development of Quality Management Systems, including documentation, change control, internal auditing and routine compliance to cGMP. Contract GMP AuditingWe offer a complete contract GMP auditing service, from first contact to report and follow up. Alternatively, a partial service can be designed to fit your requirements. GMP audits conducted of your contractors site, processes, systems and procedures, to applicable cGMP standards:Raw materials, excipients, contracted intermediates and APIs Product intermediates, bulk products, finished products Quality Risk Assessment (Gap analysis) for continuous improvement of Quality systemsQA Auditor TrainingWe offer a two- or three-day QA Auditor Training course to improve standards and gain business advantage from your Self Inspections, QA-led audits and contractor/supplier audits. Targeted at QA auditors, production/engineering managers and supervisors, plus auditors of suppliers and contractors, training may be in-house, at your chosen location.GMP Training Courses (On-site)We offer variety of On-site GMP topics to meet the current changes in regulatory requirements an