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adWatch-AE (Safety Reporting) by Atlant Systems
Adverse Event management and reporting
- Business Need
- Project Management
Helps pharmaceutical organizations to manage Adverse Events that occur during clinical trials. Gives the reporter at a clinic, hospital, investigative site an effective tool to manage AERs and report to the regulatory departments and government agencies.
Highlights
Generating, managing and reporting of Adverse Event Reports (AERs)
Provider Details
To offer life sciences companies, such as biologic, medical device, and pharmaceutical manufacturers and contract research organizations, the highest quality, most technologically advanced, and configurable business solutions and procedures to address their unique requirements. Utilizing our clinical expertise and the latest technology, we provide collaborative tools to accelerate clinical research, management of clinical trials, project management, and regulatory oversight. To provide manufacturers intelligent computer software tools and customized services to manage product complaints, adverse events, and regulatory reporting to monitor quality and take corrective actions. To offer a range of industries, including government, financial, insurance, and legal, solutions to meet their required levels of security and confidentiality. We offer industry-proven solutions to accelerate clinical research, facilitate project management, and meet regulatory guidelines. Proud of our successes, committed to our clients, we strive to exceed expectations.
Pricing Details
You can fully use this solution without payment.