Pharmaceutical Manufacturing: Best Practices and Compliance

Objectives:

• Understand the regulatory requirements and standards in pharmaceutical manufacturing.
• Learn best practices in pharmaceutical production and quality assurance.
• Explore strategies for maintaining compliance in manufacturing processes.
• Understand the role of technology in enhancing pharmaceutical manufacturing practices.

Regulatory Requirements and Standards

• Overview of regulatory bodies (FDA, EMA, etc.)
• Key regulations and guidelines (GMP, GxP)
• Documentation and record-keeping requirements
• Inspections and audits in pharmaceutical manufacturing

Best Practices in Pharmaceutical Production

• Manufacturing process optimization
• Equipment maintenance and calibration
• Quality control and assurance practices
• Cleanroom management and contamination control

Maintaining Compliance in Pharmaceutical Manufacturing

• Internal and external compliance monitoring
• Risk management in manufacturing
• Employee training and awareness programs
• Handling deviations and non-compliance issues

Technology in Pharmaceutical Manufacturing

• Automation and digitalization in production
• Use of data analytics for process optimization
• Implementation of AI and machine learning in quality control
• Emerging technologies in pharmaceutical manufacturing

DATE:

1ST BATCH: 14th – 17th Apr,                                        2025    

2ND BATCH:19th – 22nd Aug,                                     2025

3RD BATCH: 9th – 12th Dec,                                         2025