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Accelerating Sterile Drug Products from Formulation to IND in 16 Weeks
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Tue 21 Jul | Boston USA

Accelerating Sterile Drug Products from Formulation to IND

Exploring Integrated CDMO Approaches to Accelerate Sterile Drug Product Development and Clinical Entry

From Sterile Formulation to IND: The Phase I Sprint
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Wed 22 Jul | New York USA

From Sterile Formulation to IND: The Phase I Sprint

Sterile capacity, Annex 1 compliance, and bioavailability for complex molecules

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