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

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

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