2nd International Summit on GMP, Quality Control and Validation 2013

Key Topics

• Current GMP Guidelines for Pharmaceuticals
• Current Regulations and Quality Standards
• Modern Quality Systems & Risk Management Approaches
• The role of "C" in CGMP
• Quality Control Audit
• Inspections and Auditing
• Analytical Method Development and Validation for Therapeutic Proteins
• Legal Requirements for Medical Devices
• Novel Methods of Purification by Downstream Processing
• International Perspectives on Quality Assurance and New Techniques
• Technology Transfer for Industrial pharmaceuticals
• Food and Nutraceuticals
• Quality Management and Quality Improvement in Research

Who should Attend

Business Entrepreneurs, delegates from Pharmaceutical & Medical Devices companies, Universities, Pharmaceutical Consultants and Research institutions.