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Modified drug release - Pharmaceutics
Areej Abu Hanieh
•
Há 7 anos
Data Analysis Of An Analytical Method Transfer To
Dwayne Neal
•
Há 13 anos
CPV Acceptance Criteria and Conditions SK09Aug16
Stephan O. Krause, PhD
•
Há 7 anos
The Analytical Method Transfer Process SK-Sep 2013
Stephan O. Krause, PhD
•
Há 8 anos
Antibiotics
Naila Ansari
•
Há 9 anos
Method Validation: What Are Its Key Parameters
complianceonline123
•
Há 9 anos
Risk-based Analytical Method Validation and Maintenance Strategies SK-Sep13
Stephan O. Krause, PhD
•
Há 8 anos
FDA (invited) Presentation - Specifications and Analytical Method Lifecycle for Accelerated Biologics - FDA Headquarters 28Sep15
Stephan O. Krause, PhD
•
Há 8 anos
Analytical method transfer (module 01)
Dr. Ravi Kinhikar
•
Há 8 anos
Out of specification (oos)1
Dr. Ravi Kinhikar
•
Há 9 anos
"How to draft a PATENT Specification?"
Shivang Chaudhary
•
Há 8 anos
Quality by design vs control strategy
Surang Judistprasert
•
Há 8 anos
Statistics and modelisation for QbD
AlainPoncin
•
Há 14 anos
Qbd1
ceutics1315
•
Há 9 anos
QbD @ Continous Improvment
Santanu Roy
•
Há 7 anos
Process Analytical Technology
Kim Santos
•
Há 11 anos
QbD and PAT Presentation
sunp994
•
Há 8 anos
Quality by design for Pharmaceutical Industries: An introduction
Covello Luca
•
Há 8 anos
First Step in QbD - How to Get it Right
Sun Kim
•
Há 9 anos