Webinar
On Demand Webinar – Selecting and Implementing a LIMS for a Pharma QC Laboratory
On Demand Webinar Overview
In this webinar, we will explore the benefit of LIMS to most pharmaceutical manufacturers has largely been for compliance support. Whilst this is largely the case the standard now requires a fully electronic solution, with more automation and better data.
In this webinar we will show what this solution typically looks like and how pharmaceutical manufacturers should plan for its implementation.
Key takeaways:
- The Business Requirement and Technology(s) Selection
- Validation Considerations and Planning
- Data Organization Practice
- Solution Integration and making Data Available for Analytics
- The Project Plan and Phasing its Implementation
FEATURED CASE STORY
Case Study: LabWare Centralized Data Review for a Global Biopharmaceutical Company
Overview A global biopharmaceutical company specializing in discovery, development,... LEARN MORE
FEATURED WHITE PAPER
White Paper: Managing Data Integrity in FDA-Regulated labs.
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