Maintaining logbooks are painful but necessary activities that often take up valuable time and resources. Pharmaceutical, biotech, medical devices, and other organizations that have GMP operations are turning to technology to simplify documentation, but not all approaches are equally effective.
Take a coffee break and join Gilad Langer from Tulip as he discusses Tulip’s approach to simplify documentation for regulatory compliance with data from humans, equipment, machines, and processes.
During this webinar, you’ll learn:
- Common requirements for documentation solutions for life sciences
- Why Tulip’s validatable, configurable platform is ideal for life sciences
- How Tulip is used by top pharma, biotech and medical device companies
Manufacturing Practice Lead, Tulip
Product Marketing Manager, Tulip