Online Business Applications, Inct
|Online Business Applications|
|Headquarters||9018 Heritage Pkwy Woodridge, IL 60517 United States|
|Number of employees||11-50|
For thirty years, Online Business Applications has been committed to providing advanced software solutions for the Pharmaceutical, Biotechnology, and Medical Device industries in the areas of Medical Communications and Drug Safety. We utilize proven leading-edge technologies, anticipate our clients' needs, and deliver solutions that exceed expectations, making us the medical communications software provider of choice.
At Online Business Applications, client support and customer service are our number one priorities. OBA's knowledgeable and highly qualified technical team is available to provide our clients with support for all of their IRMS-related needs. We assist with the installation, implementation, training, and daily use of IRMS, in addition to any other technical needs related to IRMS business processes.
- IRMS/Medical Information
- Adverse Events
- Content Management
- Mobile Application
- Web Based Case Entry
- Quality Assurance
- Product Complaints
IRMS-AE - Adverse Event Reporting Software
A Full Drug Safety System
IRMS-AE is our comprehensive, feature-rich, drug safety system. It can fully handle all adverse event reporting including MedWatch, CIOMS and periodic reports.
Features include full metrics reporting, tracking and querying capabilities, follow-up reports, advanced product and event capture capabilities and MedDRA and WHO Drug Dictionary integration.
Electronically Send Requests with E2B
IRMS-AE uses E2B to send requests electronically to the FDA or other drug safety systems. Comprehensive, collaborative and user-friendly periodic AE reporting encompassing PSUR, ASR, DSUR, PADER and more reduces the time required to produce periodic submissions while increasing their accuracy.
IRMS-AE Key Features Include:
- Ability to generate full MedWatch, Periodic, CIOMS and PSUR reports
- Fully 21 CFR Part 11 compliant, IRMS has full audit trails and user logs
- Complete security control and required fields managed through system parameters
- Advanced product and event capture capabilities
- MedDRA and WHO Dictionary integration
- E2B submission to the FDA
Advanced AE Case Management provides:
- Individual tracking of each report
- Advanced data management for follow-ups
- Lock dates for periodic reports