|
|
White Paper Description
Software validation is required by any company covered by the US Food, Drug and Cosmetic Act and 21 CFR Parts 210 & 211. Many small to mid-sized companies see this as an overwhelming task, but when approached in a logical manner, it does not have to be. This white paper will guide you through ten steps in making your validation run more smoothly and successfully.
Related Topic: Testing
Related Keywords: FDA validation, ERP, pharmaceutical, manufacturing, regulations, 21 CFR Part11, software validation, cGMP, validation plan, enterprise resource planning
Source: ProcessPro Software
|
10 Steps to Software Validation for Small to Mid-sized Companies
