|
Clinical application
development requires more than technology resources.
Delta has extensive experience within the Pharmaceutical
industry, strong product knowledge with systems
such as Oracle Clinical & Documentum and key
partnerships with IBM & BEA. These assets
enhance Delta’s ability to complete application
development programs that meet regulatory requirements
and streamline the drug development process. Delta
assists with numerous programs including Electronic
Data Collection (EDC), web-enabled data collection
(subset of EDC), online regulatory monitoring
& management, web-based surveillance study
management, trial data access, recruitment consent,
and more. Some of the resources we can provide
within our Clinical Development Practice include:
• SAS Developers
• Documentum Developers
• Oracle Clinical Developers
• Project Managers & Analysts
In addition to staff augmentation and providing
subject matter experts, Delta can assist with
full life cycle initiatives by managing and implementing
your technology solution or providing a hybrid
team to jointly define, design, develop and deploy
your applications.
Delta also offers prepackaged web-based frameworks
and software solutions to support and provide
a robust online solution to Surveillance Study
Management. This secure online solution enables
organizations to manage the full life cycle of
study startup via an online system including document
management, workflow, document search and retrieval,
online audit trails and reporting.
Contact
a Delta Associate to learn more about our
Clinical Development capabilities or schedule
a demo of Delta’s Surveillance Study Manager.
Please call us toll-free at (877) DELTA10.
|
