Paul Irving MD to present on the importance of Electronic Production Records, including a GAMP based Data Governance and Integrity approach at COPA-DATAs Innovation event on Life Sciences Track

Paul Irving has extensive experience as a compliance and validation consultant in the Life Science industry. He specializes in information management, creation and implementation of data integrity program, as well as in the validation of computer systems. He also has experience in all aspects of quality control, including statistical process control and the development of management information systems, gained while working at Kimberley-Clark.

At the event on the 6th October, Paul will be sharing his knowledge with a presentation detailing how Electronic Production Records (EPR), drive digital maturity within life sciences organizations by:

• Streamlining Data Capture, Integrity, and Management.
• Enhancing Compliance and Traceability.
• Improving Operational Efficiency e.g., loss prevention and real time monitoring.
• Providing better Insights Through Data Analytics.

Some of the key take aways from Paul's presentation will include

• How to apply current ISPE GAMP and Pharma 4.0 Guidance within your organization and be Inspection Ready
• How COPA_DATA - Zenon Platform can act as an enabler for Data Integrity by Design and integration to other systems, within your different levels of automation.

The meeting is Free to Attend with limited availability, attendees will be able to gain key insights into Life Sciences Manufacturing, and Paul is looking forward to meeting attendees at the event in London.