| Drug
safety is our name!
Exceptional pharmacovigilance begins at
the individual case report level with high-quality,
consistent data capture and management practices.
With today’s expanding regulations
and growing enforcement, it is more important
than ever to utilize proven methodologies
and best-practices for managing your adverse
event case load. This is why DSA’s
experience matters.
 With
DSA, you have access to the tools and experience
to provide a fully compliant and comprehensive
drug safety program, and a wide array of
pharmacovigilance services. From clinical
trials safety to post-marketing surveillance,
DSA manages data collection, triage, tracking,
and reporting of your adverse events from
start to finish.
The secret to exceptional pharmacovigilance
lies with high-quality, consistent data
management practices. In order to analyze,
assess and report important safety data,
one must use best practices for data entry,
follow-up and query, quality control, medical
review and quality assurance. DSA adheres
to industry-recognized best practices for
data management, coupled with thoughtful,
business metrics and workflow for enhanced
efficiencies.
With thousands of adverse event cases processed
each year, DSA provides unprecedented safety
support. DSA manages all aspects of adverse
event reporting including data collection,
triage, tracking, and reporting from start
to finish for both clinical and post-marketing
products. After all, Drug Safety is our
name!
DSA offers case management in the following
areas:
Contact
us to learn more about out services
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