Get Started with Ennov InSight 7.3

Ennov InSight License Components

The Ennov InSight components enable different organizational roles and functions within the regulatory lifecycle of a drug product. Each component focuses on one particular area of expertise and includes the ability to control access permissions within the component for specified users and groups.

By assigning access permissions to users or roles, you can enable some users to merely observe or access queries and summaries while enabling others to perform the daily operations of project management, research, planning, and publishing.


Available Components	Description
Ennov InSight Workflow Integration	Enables you to utilize client-specific workflows that contain multiple activities, with dependencies and preset fields, that guide processes within the system.
xEVMPD	Enables you to capture, maintain, and submit data about pharmaceutical products to comply with the Extended EudraVigilance Medicinal Product Database (XEVMPD) directive.
IDMP	Enables you to capture, maintain and submit medicinal product data to comply with the extended IDMP functionality.
Registration Planning and Tracking	(RPT) enables you to plan registration activities and collect registration data without product formulation details. It improves affiliate communication, enables you to track the status of overall global product registration activities, and maintain product registration compliance.
Product Detail Management	(PDM) enables you to track product formulation and SPL exports. It also provides queries about where products are registered and other registration information.
Submission Planning and Tracking	(SPT) enables you to create, review and track submissions from planning to publishing. It also automates assembly creation and enables you to monitor the authoring process.
Registered Document Analysis	(RDA) leverages lifecycle submission information to enhance the DMS repository for better decision support based on usage information. It enables you to query for the external approval status of documents and to perform impact analysis of registered document changes.
Electronic Lifecycle Publishing	(ELP) simplifies eCTD creation and is required to publish assemblies as eCTD submissions.
Paper Review Publishing	(PRP) enables you to build assemblies for publishing to paper. PRP enables you to add paper elements such as TOCs, cover pages, overlays, and cross references to electronically published submissions suitable for generating study report submissions, hybrids, and other electronic submission formats. Using both the ELP and PRP licenses enables you to add these publishing elements to eCTD lifecycle submissions. Finally, PRP also enables you to publish an entire assembly to a single file electronically.

JavaScript must be enabled in order to use this site.Please enable JavaScript in your browser and refresh the page.

Ennov InSight License Components

The Ennov InSight components enable different organizational roles and functions within the regulatory lifecycle of a drug product. Each component focuses on one particular area of expertise and includes the ability to control access permissions within the component for specified users and groups.

By assigning access permissions to users or roles, you can enable some users to merely observe or access queries and summaries while enabling others to perform the daily operations of project management, research, planning, and publishing.


Available Components	Description
Ennov InSight Workflow Integration	Enables you to utilize client-specific workflows that contain multiple activities, with dependencies and preset fields, that guide processes within the system.
xEVMPD	Enables you to capture, maintain, and submit data about pharmaceutical products to comply with the Extended EudraVigilance Medicinal Product Database (XEVMPD) directive.
IDMP	Enables you to capture, maintain and submit medicinal product data to comply with the extended IDMP functionality.
Registration Planning and Tracking	(RPT) enables you to plan registration activities and collect registration data without product formulation details. It improves affiliate communication, enables you to track the status of overall global product registration activities, and maintain product registration compliance.
Product Detail Management	(PDM) enables you to track product formulation and SPL exports. It also provides queries about where products are registered and other registration information.
Submission Planning and Tracking	(SPT) enables you to create, review and track submissions from planning to publishing. It also automates assembly creation and enables you to monitor the authoring process.
Registered Document Analysis	(RDA) leverages lifecycle submission information to enhance the DMS repository for better decision support based on usage information. It enables you to query for the external approval status of documents and to perform impact analysis of registered document changes.
Electronic Lifecycle Publishing	(ELP) simplifies eCTD creation and is required to publish assemblies as eCTD submissions.
Paper Review Publishing	(PRP) enables you to build assemblies for publishing to paper. PRP enables you to add paper elements such as TOCs, cover pages, overlays, and cross references to electronically published submissions suitable for generating study report submissions, hybrids, and other electronic submission formats. Using both the ELP and PRP licenses enables you to add these publishing elements to eCTD lifecycle submissions. Finally, PRP also enables you to publish an entire assembly to a single file electronically.