| Name of Product/Service |
| Company Name |
| Company Location |
Copenhagen, Denmark |
| Company Website |
http://www.tarius.com |
| Product/Service Website |
http://www.tarius.com/Indhold/Subscriptions.aspx |
| Status |
Commercial Service |
| Launch Date |
January 1995 |
| PSI Sector |
Healthcare |
| Main Source of PSI Re-used |
Regulatory databases containing US and EU regulations for professionals involved with legislation for medical devices and human drugs.
Products include:
Tarius Base Module: Medical Devices
Data is sourced from:
- US Legislation
- US Code of Federal Regulations
- FDA Reference Documents:
- FDA Advisory Committees
- US NIST
- US-EU Authorities’ Cooperation
- EU Regulations and Directives
- EU Commission and EU Council Decisions, Communications and Guidelines
- GHTF: (Global Harmonization Task Force regarding Medical Devices)
- Eucomed
-
ISO Standards
Tarius Base Module: Human Drugs
Data is sourced from:
- US Legislation
- US Code of Federal Regulations
- US FDA Reference Documents:
- US DEA Reference Documents
- US Agreements with other countries
- EU Regulations and Directives
- EU Commission and EMEA Reference Documents
- EU CMD(h) Documents
- EU agreements with other countries
- ICH
- PIC/S and WHO
-
BIO, EFPIA, PhRMA and IPPMA
|
| Value Added to PSI |
Product features include:
- Global intelligence – allows searching across US and EU regulations in one operation
- Daily updates – new publications are automatically added to subscriptions on a daily basis
- Weekly email alert – for registrants
- Clear indication of document status - whether "draft", "in force" or "superseded",
- Thematically organized – the detailed table of contents allows step by step navigation.
- Highlighted search terms in documents - opening a document from the Search Hit List, search terms are automatically highlighted
|
| Description of the Business and Role of PSI |
Tarius is a wholly owned subsidiary of The Schultz Group.
Tarius has, since 1995, provided professionals in the pharmaceutical, biologics and medical device industries with the information they need to remain compliant in global markets.
|