See what a validation package looks like when it builds itself
A short walkthrough of how GxPForge keeps traceability current as your team works, instead of reconstructing it before a release.
Book a demoGxP is shorthand for good practice, with the x standing in for whichever discipline is being discussed, manufacturing, laboratory, clinical, distribution, or documentation. It is not one rule. It is a family of related regulatory expectations that all share the same underlying goal, product quality and patient safety.
Across every flavor of GxP, the underlying expectation is the same. Processes should be defined in advance, followed consistently, and documented in a way that lets someone reconstruct what happened later. A system, a person, or a process that cannot show this trail is, functionally, not compliant, even if the outcome happened to be fine.
GMP covers manufacturing. GLP covers non clinical laboratory studies. GCP covers clinical trials. GDP covers distribution and storage. GVP covers pharmacovigilance. A single company can be subject to several of these at once depending on what it makes and how it moves product through its supply chain.
Any system that touches a GxP relevant record or decision inherits the same expectations, which is where computer system validation comes in. The system itself becomes part of the evidence chain, and it has to hold up to the same scrutiny as a paper process would.
A short walkthrough of how GxPForge keeps traceability current as your team works, instead of reconstructing it before a release.
Book a demo