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Modified drug release - Pharmaceutics
Areej Abu Hanieh
•
il y a 7 ans
Data Analysis Of An Analytical Method Transfer To
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il y a 13 ans
CPV Acceptance Criteria and Conditions SK09Aug16
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il y a 7 ans
The Analytical Method Transfer Process SK-Sep 2013
Stephan O. Krause, PhD
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il y a 8 ans
Antibiotics
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il y a 10 ans
Method Validation: What Are Its Key Parameters
complianceonline123
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il y a 9 ans
Risk-based Analytical Method Validation and Maintenance Strategies SK-Sep13
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il y a 8 ans
FDA (invited) Presentation - Specifications and Analytical Method Lifecycle for Accelerated Biologics - FDA Headquarters 28Sep15
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il y a 8 ans
Analytical method transfer (module 01)
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il y a 8 ans
Out of specification (oos)1
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il y a 9 ans
"How to draft a PATENT Specification?"
Shivang Chaudhary
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il y a 8 ans
Quality by design vs control strategy
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il y a 8 ans
Statistics and modelisation for QbD
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il y a 14 ans
Qbd1
ceutics1315
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il y a 9 ans
QbD @ Continous Improvment
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il y a 7 ans
Process Analytical Technology
Kim Santos
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il y a 11 ans
QbD and PAT Presentation
sunp994
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il y a 8 ans
Quality by design for Pharmaceutical Industries: An introduction
Covello Luca
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il y a 8 ans
First Step in QbD - How to Get it Right
Sun Kim
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il y a 9 ans
FMEA, DoE & PAT : Three Inseparable Organs of Quality Risk Management (QRM) Body for Pharmaceutical Product Development with QbD
Shivang Chaudhary
•
il y a 10 ans