Are you constantly gowning up to go from one clean room environment to another, to get signatures on SOPs, master records, controlled documents, etc. only to realise that the paper copy is out of date, or is missing a page, and you need to start the signature gathering all over again?
Do you ever wonder why, in this day and age, working for a high tech pharma or biotech company, you’re still carrying stacks of paper around?
Download this webinar featuring industry leader Biogen Idec to learn how to save time, money, and materials and increase compliance across Manufacturing by leveraging QUMAS Quality and Regulatory Compliance Management Software on Apple iPads.
This webinar will detail how Biogen Idec has taken Manufacturing from paper to electronic with topics including:
- Review of old paper methods
- Piloting of devices
- User acceptance feedback
- Implementation plan
- On-going enhancements
- Gregory Chua, Senior Manufacturing Support Associate, Biogen Idec
- Murtuza Vasowalla, BIOVIA, Director, Global Solutions Consulting
Duration: 56 mins