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Quality-by-Design In Pharmaceutical Development: Introduction, ICH Q8 guideline, Regulatory and ind...
IPQC & FPQC of pharmaceuticals
A detailed study on the guidelines that are taken for ICH which is also known as the International C...
The presentation gives an insight on BABE studies, mathematical and statistical procedures involved ...
Parenterals: An In-Depth Overview
Elimination Bioavailability and �Bioequivalence Factors Affecting Renal Excretion or Renal Clearan...
Brief overview of stability testing and its protocol to be followed for stability testing for herbal...
Evaluation of Ophthalmic preparation
This presentation covers the ICH guidelines coding no in details.
Regulatory requirements of BIOAVAILABLITY & BIOEQUIVALENCE STUDIES
Ipqc for tablets
Tablet production process
Hard gelatin capsules: Introduction, Extraction of gelatin and production of hardgelatin capsule she...
In this slide contains Quality-by-Design in Pharmaceutical Development. Presented by: T. MOUSAMI BH...
EUTECTIC MIXTURE, APPLICATION OF EUTECTIC MIXTURE IN PHARMACEUTICAL INDUSTRY:
The chapter deals with the preformulation studies that have to be considered while designing a dosag...
Lyophilization or freeze drying is a process in which water is removed from a product after it is fr...
QCM, quality control managment
Introduction Overview: The role of physical properties in drug design is crucial for the developmen...
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detail about preformulation study
Unit II, Industrial Pharmacy III Year , Semester - V