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| > > > GRRT |
 Global Regulatory Requirement Tracking (GRRT) |
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The pharmaceutical industry is constantly being challenged to meet increasing regulatory requirements. These compliance
regulations are extremely complex, change frequently and are difficult to monitor.
The DoubleBridge Technologies, Inc. Regulatory Requirements Tracking system provides a secure, up-to-date library of
country specific regulatory requirements and procedures, which can be used by multinational corporations.
Features:
Monitors activities of government agencies such as FDA, EMEA, and PMDA.
Includes pre-built and ad-hoc reports.
Tracks regulatory requirements for all stages of the drug development process.
Monitors regulatory requirements for various submission types including IND, NDA, and Device.
Tracks regulatory procedure, sample, certificate and dossier requirements.
Benefits:
Permits company-wide database usage.
Allows configurable user access and security features.
Allows configurable country and regional options.
Facilitates easy access to required information.
Reduces approval times.
Reduces compliance violations.
Streamlines submission process and time to market.
Back to iPharmaTrack
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