Ennov InSight Registrations Best Practices

The best practice topics provide recommendations to help you take advantage of built-in efficiencies in Ennov InSight .

The following topics are intended to be used in conjunction with the Ennov InSight user documentation. They provide best practice and process recommendations for using the Ennov InSight suite to create and manage eCTD submissions to regulatory authorities. These provide general best practice guidelines and module-specific tips and tricks to best leverage the lifecycle management aspects and assembly features of the Ennov InSight suite. It is not intended to replace the user documentation. Specific details on how to perform individual functions are included in the online help, not in these Best Practice guides. For Publishing Best Practice guides, See Publishing Best Practices.


Name
Associating SPOR Values in Data Admin
CE Mark Applications
Consumer Product Applications
Creating EU PSUR Events
Creating Flu Vaccines
EAEU Procedures
GCC Procedure
Guide to Managing BREXIT Related Regulatory Activities
Internal and External Status Values
Linked Systems
Management of Change
Managing Active Ingredients for XEVMPD Submissions
Managing Users Best Practice
MRP and DCP Variations Approvals
Named Patient Program and Import License
Orphan Drug Designation
Pediatric Plans
Plasma Master File
PMS Data Enrichment
Power Search
Risk Management Plan
Submitting products pending approval to XEVMPD
Substance Registration (DMF, CEP, ASMF)
Sunset Clause Reporting
User Activity Report
Using the Association Closed As Functionality
Withdrawing Products