Welcome to the Delphi Analytical Services, Inc. Online Store!
We offer regulatory compliance templates, books, manuals, handouts, and "on demand" consulting services to help you avoid regulatory entanglements with FDA!
**Delphi Analytical Services, Inc. is Proud to Announce that 2015 Marks Its 16th Year in Business**
CGMP Consulting Services
In order to better service our non-regional and international customers, Delphi Analytical Services, Inc. is now providing “on demand” consulting services. Offering a substantially discounted rate we can now provide “off site” consulting services to the pharmaceutical, biotech, medical device, contract analytical, contract manufacturing, and related industries. This may take the form of telephone, e-mail, and live video conferencing (a .Mac or AIM account and web camera is required) or a combination of all. We can assist you with issues related to compliance with 21 CFR Parts 210, 211, Current Good Manufacturing Practices for Finished Pharmaceuticals and 21 CFR 820 the Quality System Regulations for Medical Devices. The majority of our experience is based in helping companies under Consent Decree with the FDA or who are trying to prevent regulatory entanglements with agency. We also have substantial experience with small business start up as well as companies which provide products and services to the industries mentioned above. Services can be purchased for $200/hour, with a one hour minimum order and are deducted in .25 hour minimum increments.