Life Sciences GxP Training From a Regulatory Perspective

Onboarding new employees and upskilling existing ones on Standard Operating Procedures (SOP) and Current Good Manufacturing Practice (cGMP) is mandatory to ensure personnel involved in pharmaceutical drug product manufacturing learn and adhere to the GxP procedures.

In a regulated industry so inherently regulated by regulatory agencies, life science companies often take particular care of personnel training to ensure safety and efficacy of drug products as well as to comply with the cGMP guidelines for training as stipulated by regulatory agencies.

In this webinar, you will learn about the important factors you should focus on while building your GxP training plan that meets regulatory expectations, complies with cGMP guidelines and improves training effectiveness.

You will also learn about the key steps to take when preparing your annual GxP training plan. Some key points we’ll discuss include:

• What are regulatory expectations for GxP training
• Common mistakes to avoid
• Moving from checklist-based compliance training to a performance-based learning
• Quality Metrics for learning effectiveness
• How digital learning technology can help

Speaker

Dr. Mark Lee, senior business development manager, ComplianceWire, UL Solutions