Embase Supports the Post-Market Team

What do you need?

• You need to keep up with the changes in reporting regulations.
• You need to track adverse drug information reported for your drug, and your competitors’ drugs, and report in adverse events case report, or a periodic safety update report (PSUR).
• You need to keep on top of the growing pool of preclinical information and clinical trial data for your drug to submit a successful New Drug Application (NDA).

Embase has the answers

• Embase helps you keep up to date by giving you access to conference abstracts, as well as drug-related journals, including some not listed in Medline.
• In-depth indexing using Embase’s drug toxicology and clinical trial subheadings will find any reports of side effects information.
• Our RSS feed and email alerts mean that you won’t miss a thing.

To Learn how Embase Supports the Post-Market Team, contact us today