Consultant Services We have Consultant Services in the following areas Manufacturing & Import Authorization (MIA) in Europe Pharmaceutical Quality System Compliance Qualified Person & Batch Release Services Preparation for National and International Authorities Inspection Proper CAPA handling Services for responding to an Inspection report
Training programs We have a range of professional courses and training programs that could be tailored based on the client’s needs: In-House training Scheduled training EU GMP for Beginners EU GMP for Professionals GDP for API GDP for Finished Product
Audit Services We have different Audit Services GAP Analysis of PQMS of pharmaceutical organization Reviewing PQMS Indicating the GAPS Supporting to take relevant actions for closing GAPS Promoting Development Internal & Mock Audit: Reviewing your documents before submission In house or virtual Audit, in agreed scheduled time Providing a detailed professional Audit Report Following up for CAPA plan and closing observations Promoting Development and closing observations Supplier Qualification In house or virtual Audit, in agreed scheduled time Providing a detailed professional report Supplier Questionnaire Supply chain map QP Declaration
Consultant Services We have Consultant Services in the following areas Manufacturing & Import Authorization (MIA) in Europe Pharmaceutical Quality System Compliance Qualified Person & Batch Release Services Preparation for National and International Authorities Inspection Proper CAPA handling Services for responding to an Inspection report
Training programs We have a range of professional courses and training programs that could be tailored based on the client’s needs: In-House training Scheduled training EU GMP for Beginners EU GMP for Professionals GDP for API GDP for Finished Product
Audit Services We have different Audit Services GAP Analysis of PQMS of pharmaceutical organization Reviewing PQMS Indicating the GAPS Supporting to take relevant actions for closing GAPS Promoting Development Internal & Mock Audit: Reviewing your documents before submission In house or virtual Audit, in agreed scheduled time Providing a detailed professional Audit Report Following up for CAPA plan and closing observations Promoting Development and closing observations Supplier Qualification In house or virtual Audit, in agreed scheduled time Providing a detailed professional report Supplier Questionnaire Supply chain map QP Declaration
February 3, 2022 admin Uncategorized Hello world! Welcome to WordPress. This is your first post. Edit or delete it, then start writing! Read More
March 22, 2018 admin Industry Global Automative Market Grows to $600 billion Lorem ipsum dolor sit amet, consectetur adipiscing elit possim mei ludus. Proin sedi diame sapien errem eleifend definitionem semper urna dict. Pellentesque ornare sem lacinia quam venenatis vestibulum. Read More