The ultimate tool for research on domestic pharmaceutical compliance policies and regulations
The Pharmaceutical Regulation Suite provides easy, convenient access to huge volumes of complex information related to domestic pharmaceutical compliance policies. Consolidated, Web-based tools speed research through thousands of federal publications, guidance documents, reports and other regulatory resources.
- Stay current with FDA approvals and enforcement activities
- Easily access information on thousands of drug and biologics products and companies
- Get continual updates from the regulatory agencies involved in drug enforcement and regulation
- Eliminate months of waiting for responses to Freedom of Information (FOI) requests.
Complete, consolidated pharmaceutical compliance policies and resources
The Pharmaceutical Regulation Suite gives you quick access to the most complete collection of regulatory and pharmaceutical compliance policies possible, including some not available on the Web. Resources span many agencies and document types.
- Code of Federal Regulations, including 21 CFR and eleven other titles, updated continuously
- Federal Register, updated daily, with archives back to 1991
- U.S. Code and public laws
- Import Alerts in a table sortable by date, alert number or title/description
- CDER monthly generic drug approvals and Orange Book
- FDA Freedom of Information (FOI) Logs
- Press releases, speeches, testimonies and forms
- Safety information and drug safety labeling changes
- FDA manuals and guidance documents, including the CDER guidance database
Quick access to data
The Pharmaceutical Regulation Suite allows you to get all the information you need using a single set of integrated, robust search tools. Easy Web links, extensive archives and fast searches save time and connect you quickly to key regulatory information.
- Automatic daily updates
- Easy searches from a single location
- Fast, easy-to-use search tools