Thermo Fisher Scientific Expands its Global Biologics and Steriles Manufacturing Capabilities in China
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Risk assessment strategies in oral solid dosage development and manufacturing
Webinar On Demand
When you reach each stage in your drug development journey, there are numerous items to look out for as you look to scale up your product. From early development to commercial scale, the potential impact of changes in your API and drug product formulation should require a best foot forward strategy.
Watch this on demand webinar to learn more about:
- Performing risk assessments by development stage
- Tools that can be used to de-risk during drug development
- What to look out for post phase I
- Getting ready for process validation and registration
Author:
Andrew Horler
and Kevin Kane, PhD