Event Details

When

Wednesday, 23 June - 2pm-3pm

Where

Online

Life science organisations who develop, manufacture and supply drugs and medical devices operate in a highly regulated environment. QA audits and inspections play a vital role in maintaining the highest quality standards during trials and production.

As virtual audits and inspections become the “the new normal” there is a need to manage regulated content at the time of collection, storage and processing for businesses to fully benefit from this new methodology. 

Lifescience Industry News has been looking at how Box can support the transition to virtual audits and inspections, with the ability to effortlessly manage the delivery of secure, inspection-ready, standards-compliant documentation from collection to the auditor’s desktop.

Programme

• Introduction - Audits and Inspections

• Regulatory perspective

• PCI - Supplychain perspective

• Covance - CRO perspective

• Box - Digital solutions

Chair: Gwyn Tudor, Lifescience Industry & MediWales