Tarius Web Portals have continued to win growing acceptance among globally leading pharmaceutical companies. And soon, with the launch of a web portal for medical devices, even more companies will be able find the answers they need to their regulatory questions.
Tarius' new Medical Device Web Portal is being co-developed with GE Healthcare, Waukesha, WI.
Tarius is expanding its coverage to include Medical Devices/IDVs already this summer!
Global coverage
Tarius offers global coverage of more than 60 countries, regions and international organizations, including Latin America, North America, South Africa, Middle East, Eastern and Western Europe, South Asia, Southeast Asia and The Pacific Rim. Because this up-to-date intelligence is available from a single site, Tarius not only promises to minimize the amount of time spent on searching and preparation, it can help assure that the quality and reliability of the information collected meets the quality and accuracy standards required by the healthcare industry.
Customized
The Tarius Web Portal allows your company to choose which countries you want to include in your company web portal. In addition, the customized web content will focus solely on your company's product lines, eliminating the need to spend hours searching multiple web sites or through cumbersome data sources.
"Google-like" ease of use
Tarius offers the power and user-friendly functionality to help you quickly find, use and share the exact information you need. Equally important, all data has undergone strict quality checking. This means professionals can be confident that Tarius information is completely accurate, reliable and up-to-date.
For Drugs, Medical Devices or both
Today, companies are challenged to get regulatory approvals for an ever-increasing number of products each year. At the same time, they often have to do so with fewer resources. This "do more with less, faster" directive challenges the employees to improve process capabilities, eliminate unproductive steps and reduce the risk of making decisions based on unreliable or incomplete information.
A customized Tarius portal for drugs, medical devices or both can help you do exactly that. It will ensure that your regulatory affairs and quality professionals get the up-to-date information needed to stay on top of the current regulatory landscape in the US, EU, Asia, Latin America and other regions of the world.
Updated daily so you can make better decisions faster
Tarius is a convenient, one-source web portal that provides the medical device professionals access to up-to-date information, including:
1) Expert summaries describing medical device regulatory FAQ's
The summaries are written by Tarius' network of national, independent experts and consultants. The summaries describe business-critical issues such as: national registration or licensing processes, questions related to medical device classification, procedures for scientific advice and clinical trials of medical devices, labelling, import/export regulations, etc.
2) Reference documents from national authorities
Tarius systematically monitors national governments' and relevant national authorities' websites to provide organized compilations of: acts, regulations, directives, codes, decisions, policy papers, guidelines, warning letters, press releases, forms, and more.
English metadata are added to each of the national documents (title, keywords, abstract, etc), enabling effective search in English - even if the original document is in non-English language. Previous and superseding versions are easily found via hyperlinks.
Reference documents are monitored continuously and updates are uploaded to the web portal on a daily basis.
Test drive Tarius for free!
To request a free trial of the new Web Portal for Medical Device companies, sign up here.