WIS Co. publishes Warning Letter Bulletin, a monthly newsletter that summarizes all Food and Drug Administration (FDA) "warning letters" and "untitled letters" to manufacturers of drugs, devices, animal drugs, foods, dietary supplements and blood products; Food & Drug Inspection Monitor, a monthly newsletter that analyzes FDA inspections of drug and device manufacturers and blood banks; GMP/Supply Chain Report (formerly, Validation Times), a bi-weekly PDF newsletter focused on drug GMPs, supply chain integrity and efforts to thwart diversion and counterfeiting; and Adverse Event Reporting News, a biweekly publication delivered in PDF format, which monitors FDA and EU regulation of adverse event reporting, pharmacovigilance and complaint handling.
All subscribers can use WIS' RECORD-RETRIEVE Document Retrieval & Research Service -- www.FDADocuments.org -- which provides documents from FDA or any other government agency for a fee.
All WIS newsletters are available on-line through through The Gale Group.
WIS also publishes the following books and electronic products: 510(k)s/PMAs on DVD, Warning Letters on DVD, Complete Validation Handbook, Pharmaceutical Supply Chain Compliance Manual, FDA Computer, Software & Cyberseurity Manual, FDA Guide to Systems-Based Inspections, 483s and EIRs on DVD, REMS Handbook. FDA documents are listed on the World-Wide Web, WWW.FDAINFO.COM.
WIS also provides information to the news media and consumers on an as-needed basis.
WIS is an independent publisher. It is incorporated in the state of Virginia, with offices at 19-B Wirt Street, Leesburg, VA 20175