The two-day conference will help you discover how recent technological advances are revolutionizing Pharmaceuticals & Biopharmaceuticals manufacturing and quality compliance and how it represents a significant opportunity to enhance overall efficiency, quality, responsiveness, regulatory compliance, and sustainability. You will learn about new technologies, implementation challenges, regulatory expectations, other key factors and moving forward how these insights will reshape the industry landscape and improve patient safety.

The conference will mainly focus on advanced technologies used to improve the various manufacturing process. The main focus areas of the conference will be -

• Annex 1 & Containment requirements
• Containment for high potent products
• CCS & Quality Risk Management
• Engineering of Contamination Control
• Leveraging Digitization to Reduce FDA Recall Risks
• Regulatory update on Biotechnology products
• ADC purification: challenges and solutions
• Case study of Fill finish for high-potent ADC
• Closed Processing for Next Generation Biomanufacturing
• Plastic Waste Quantitation in Biopharmaceutical Manufacturing
• ATMP Manufacturing
• Airflow Visualization techniques & technology
• Unique application of lyophilization for Pharmaceuticals
• Sustainability in Digitalization and Automation
• Practicing Annex 1 in Sterile environment

During the two day conference Mr. Sadiq Khan, Director Region IMEA, will share his insights on the need of the hour topic

DIGITAL TRANSFORMATION WITH ASSET ADMINISTRATION SHELL FOR EFFICIENCY IMPROVEMENT

To know more about the conference and participation. Click here