Asset Visibility: Pharma Industry Track and Trace Regulations in Europe
Price:
Starting at USD 3,000
Publish Date: 13 Feb 2022
Code: PT-2570
Research Type: Presentation
Pages: 23
Actionable Benefits
- Strategic planning for pharmaceutical vendors and distributors for changes in serialization regulations.
- Gain insight into scale and scope of regulations.
- Guidance into proposed future regulatory changes.
Research Highlights
- Regional focus on Europe (EU, UK, Switzerland & Russia)
- Identifies variation between European Union regulations and other European regions.
- Comparison and analysis of different levels of traceability.
Critical Questions Answered
- What is the timeline for implementation of serialization regulations?
- What are the key data standards and mandates for traceability?
- How are international standards like GS1 leveraged in national regulations?
Who Should Read This?
- Strategy planners and advisors within the pharmaceutical and supporting logistics industry.
- Managers aiming to identify regulatory requirements of their operations.
- For serialization software and hardware providers to assess regulatory impact on the pharmaceutical market.