ViP is currently retained by a major pharmaceutical client to provide a range of regulatory guidance texts to support the company's day-to-day operations. These compliance guides were originally developed for in-house reference but proved so popular with our clients that we were forced to publish them. What differentiates our guidance documents from the vast array currently available is that they are simply compilations of regulatory fact, with no additional interpretation. Using our extensive regulatory database we extract all of the EC and FDA regulations, guidance and citations, associated with a specific topic and then combine them under logical subheadings in a single reference text. This provides our team and clients with a solid foundation of fact on which to base CGMP compliance decisions.