Appian is dedicated to configuring software solutions for the Li fe Science industry that satisfies Title 21 CFR Part 11 requirements as well as GxP (i.e., GMP, GCP, GLP, and GAMP). We recognize our life science clients must follow good practices (GxP) to ensure their manufacturing processes, clinical trials, technology transfer/scale ups, and postmarketing surveillance activities meet very specific compliance and quality requirements. Appian’s core architecture includes many features that assist in validation and ensuring compliance to relevant international quality standards and best practices.
How Appian Supports GxP Principles for Life Sciences Companies
