In Life Sciences, following good practices (GxP) to ensure manufacturing processes, clinical trials, technology transfer/scale ups, and post-marketing surveillance activities meet very specific compliance and quality requirements is of great importance.
Appian is dedicated to configuring software solutions for the Life Sciences industry that satisfy Title 21 CFR Part 11 requirements as well as GxP (i.e., GMP, GCP, GLP, and GAMP).
Download this whitepaper to learn how Appian:
- Makes it easy to share mid-stage development with business users
- Assists in validation and ensuring compliance to relevant international quality standards and best practices
- Helps create applications that are generally delivered with higher confidence in a shorter time period and at a lower cost