In this presentation, the speakers will discuss key findings of a customer use case that involved an SSI impact assessment for a chemical and protein substance according to the latest ISO Implementation Guideline (March 2016).
Contact the event managers listed below for more information about how you can participate at the Will Your CMC Data be IDMP e-Submission Ready by 2018?.
|Conference/Event Dates:||10/19/2016 - 10/19/2016|
|Primary Industry:||Clinical Pharmacology|
|Other Industries:||Clinical Pharmacology, Professional Healthcare|
|Audience:||Senior level professionals from biopharma companies working within:
Quality assurance / control
|Booth Size||Booth Cost||Available Amenities|
|Marketing Vehicles Allowed:||n/a|
|Other Booth Sizes Available: n/a|
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