Our new and completely redesigned R3 compliant PV database
BaseCon3 is an intuitive E2B R3 compliant pharmacovigilance and drug safety software that manages electronic AE reports reliably, smartly and quickly. BaseCon3 is completely redesigned and developed from scratch based on more that 20 years of experience.
Intuitive software
Do more with streamlined and easy-to-follow workflows, that are made to save you time.
The smart investment
BaseCon software makes pharmacovigilance practices easier to adhere to and expedites critical tasks.
Trust since 1999
BaseCon software has been the choice of pharmaceutical and CRO firms for two decades.
Intuitive software
Do more with streamlined and easy-to-follow workflows, that are made to save you time.
The smart investment
BaseCon software makes pharmacovigilance practices easier to adhere to and expedites critical tasks.
Trust since 1999
BaseCon software has been the choice of pharmaceutical and CRO firms for two decades.
Client Testimonials
Key Features and benefits
Secure AE case submission
Send and receive Adverse Event cases in XML file format (E2B R2 & R3) over a secure encrypted connection to authorities or partners and ensure quick and easy reporting in a compliant manner.
Electronic gateway included
Our integrated gateway works seamlessly with the entire database and users never have to manually track submissions. Acknowledgement files are automatically uploaded.
Automatic Receiver Selections
Users receive an automated list of report receivers to select, saving time while ensuring quality and consistency.
Fully integrated Product Register
Leverage automated product names, active substance(s), countries in which the product is marketed, labelling information and much more included in your product register during case data entry and save users time. Product information is also automatically transferred to the case.
Submissions Tracking
Easily track reports sent to partners and authorities, see time stamps and case versions with an easy-to-read dashboard, giving users the ability to comfortably meet deadlines.
Paper reports
Save time with electronically generated pre-filled standard CIOMS and MedWatch forms.
PSUR/DSURs
Save time with automated listings and summary tabulations fully compliant and ready for use in GVP Module VII reports. Tables and listing can be used for both post-marketing drug and clinical trials safety.
Real-Time Surveillance
Easily track cases, monitor safety and check for signals using up-to-date reports.
Electronic Archive
Track all received documents for unique cases using our secure case archive.
Simple and Secure Web-access
Encrypted access via a web-browser from any location
Schedule your demo
Experience the efficiency of streamlined workflows and intuitive user experience in your business.
