cGARD

cGARD (current Global Automated Regulatory Database) is an exceptionally user-friendly tool, which is available online. It brings together precise up-to-date, categorised regulatory information, ability to search for FDA Warning Letters, access to latest industry news in order to assist companies effectively coordinate their corporate regulatory intelligence requirements and stay inspection ready.

Features:
Single source of regulatory data
Available online - always up to date, no installation needed
Secure db technology - Oracle
Regulations categorised - ability to limit searches to industry-defined compliance subjects
Draft regulations
Validation Documentation Templates - FS, HATS, HDS, IQ, OQ, PQ, DQ Risk Assessment, Code Review, SDS, URS, Validation Plan, Validation Report
Change Matrix - history and details of all changes to regulations covered in the tool
Advanced keyword, keywords or phrase search facility, including bookmarking
Glossary database of regulatory, pharmaceutical and life-science terminology
Full reporting and print capability - Export of data to industry recognised file format (.doc or .pdf)
Regulatory assessment reports
Links to global regulatory agencies
Search of FDA Warning Letters
View news from trusted sources within the industry including, but not limited to, press releases, recalls information and enforcement reports from fda.gov.
Ability to add personalised content to cGARD, like ISOs, copyrighted guidelines, company corporate standards, SOPs, QMS etc. – function enabled only in a corporate version of cGARD

Link: http://www.compliance-control.com/en/cc-centre/cc-cgard.html