Some of the rules and regulations are just so essential that every RA and QA person in any pharmaceutical or medical device company must have them at their fingertips. That is why we created our Base Modules.

For some companies these are the basic rules they work on. They enjoy having them in a daily updated archive, including also superseded versions. When they need other documents they just search and download from the Internet. For other companies this Tarius compilation is just the start of specifying the contents of their company-specific online web portal.

Tarius leaves that decision to you. If you fell comfortable with the basic contents of the pre-defined compilation, it’s fine. If you need more than that, just let us know and you will have the option of selecting from our vast inventory of continuously updated "building blocks" of information. Or, you may ask us to provide web site monitoring for your eyes only.

No matter if you subscribe to our pre-defined compilations or you choose to customize a company-specific solution, you will not be troubled with IT-related issues. You just need to focus on the contents you need – the rest is handled by us.

See below for a listing of our products and services chosen especially for you:

Base Module: Human Drugs
...... a pre-defined, comprehensive and well-structured compilation of reference documents from US and EU authorities as well as from several important international bodies concerning all major regulatory, quality and compliance regulation issues for pharmaceutical and biotech companies. (more)

Base Module: Medical Devices
...... a continuously updated compilation of reference documents from US and EU authorities as well as focused selections of guidance documents and standards from important international bodies, all vital to the medical device industry. (more)

LovText Lægemidler
...... an electronic compilation of the Danish regulations on medicinal products created specifically for Danes in their native language. The product is edited in close dialog with the Danish Medicines Agency. (more)