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  • INTERACTIVE REPORT

  • Toggle navigation      
    • Introduction
    • Chapter 1
      External Drivers: Globalization and IDMP
    • Chapter 2
      Internal Drivers: Fragmentation and Inefficiency
    • Chapter 3
      The Regulatory Transformation Underway
    • Chapter 4
      Innovating with Veeva Vault RIM
    • Demo: Unified RIM

Regulatory Transformation

Expanding into new markets places a spotlight on inefficient processes, highlighting the need for greater agility and major changes to regulatory systems and processes.

Read about the drivers and trends within these RIM Transformation Initiatives.

CHAPTER
1
External Drivers: Globalization and IDMP
CHAPTER
2
Internal Drivers: Fragmentation and Inefficiency
CHAPTER
3
The Regulatory Transformation Underway
CHAPTER
4
Innovating with Veeva Vault RIM   
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Sources

  1. IMS Institute for Healthcare Informatics, Global Medicines Use in 2020, November 2015.

  2. Elements of ISO IDMP-compliant SPOR data will be used in ICSR E2B(R3), the Falsified Medicines Directive (FMD), and European Clinical Trials Database (EudraCT).
     
  3. Gens & Associates, Pursuing World Class RIM: Strategy, Measures and Priorities, November 2016.
     
  4. Ibid.
     
  5. The Vault RIM Suite includes the following products: Veeva Vault Registrations, Veeva Vault Submissions, Veeva Vault Submissions Archive, Veeva Vault Submissions Publishing.
     
  6. Major markets: United States, Canada, Japan, France, Germany, Spain, United Kingdom, Italy.
     
  7. Growth markets: China, Brazil, Russia, India, Mexico, Turkey, Poland, Venezuela, Argentina, Indonesia, South africa, Thailand, Romania, Egypt, Ukraine, Pakistan, Vietnam.
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