Regulatory Connections

Connections

RIM – Clinical Operations

Announced 2020 Status Mature Customers 50-100

Drive more efficient collaboration between clinical and regulatory teams by sharing product, study, site and submission data along with investigator CVs, 1572s, protocols, and investigator brochures.

  • Product and Study Data: Any RIM and Clinical – Sync study and product data across applications
  • Document Exchange: eTMF and Submissions – Accelerate document readiness by automating availability in corresponding system
  • Submission Tracking: SSU and Submissions – Automatically track submission data, reducing manual steps and reconciliation
Watch Demo Features Brief
Veeva Help

Vault Help

About the RIM-Clinical Operations Connection

Vault Help

Configuring the RIM-Clinical Operations Connection

Vault Help

Technical Details for Creating and Managing Veeva Connections
Customer Success Stories

Customer Story

Read Customer Success Story – Cerevel

Customer Story

Read Customer Success Story – UroGen

Additional Resources

Webinar

RIM-Clinical Operations Connection: Live Discussion Replay

RIM – PromoMats

Announced 2021 Status Mature Customers 11-50

Accelerate business operations by automating the management of documents and product data between Veeva RIM and Veeva PromoMats.

  • AdPromo Submissions: Submissions and PromoMats – Link eCTD documents in PromoMats to Veeva Submission Content Plans
  • Document Exchange: Submissions and PromoMats – Automate transfer of documents using document crosslinks from approved content
  • Product Data: Any RIM and PromoMats – Sync product data to allow marketing teams make informed decisions
Watch Demo Features Brief
Veeva Help

Vault Help

About the RIM-PromoMats Connection

Vault Help

Configuring the RIM-PromoMats Connection
Additional Resources

Webinar

RIM-PromoMats Connection: Live Discussion Replay

Quality – RIM

Announced 2019 Status Mature Customers 11-50

Automate the coordination of product change control activities by sharing critical data and documents between the Quality (QMS) and Regulatory (RIM) Vaults, speeding up regulatory assessments and ensuring compliance.

  • Product Data: Any Quality and RIM – Single source of truth for product data to ensure consistency and accuracy
  • Enhanced Change Control: QMS and Registrations – Accelerate bidirectional change controls with regulatory impact seamlessly
  • Document Exchange: Quality Docs and Submissions – Share documents across teams and eliminate redundant effort
Features Brief
Veeva Help

Vault Help

About the Quality-RIM Connection
Customer Success Stories

Customer Story

Read Customer Success Story – Sarepta

Additional Resources

Webinar

Quality–RIM Connection: Live Discussion Replay

Safety – RIM

Announced 2023 Status Early Customers 1-10

Share product and registrations data between regulatory and safety to streamline case processing.

  • Product Data: Any Safety and any RIM – enable a single source of truth for product and registration data
Watch Demo
Veeva Help

Vault Help

About the Safety-RIM Connection

Vault Help

Configuring the Safety-RIM Connection
Additional Resources

Webinar

Safety-RIM Connection: Live Discussion Replay