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Freshers in clinical research and regulatory affairs must go through this presentation. It will help...
clinical trials history and types
21 CFR 312 and 314 are two separate, but related, US Food and Drug Administration (FDA) regulations ...
Study of effects of dissolution parameters Presented by J. Lokdep Reddy Department of Pharmaceutic...
ICH Guidelines of Quality, Safety, Efficacy and Multidisciplinary guidelines that implemented by Int...
This presentation covers the ICH guidelines coding no in details.
1.Patients have poor or no knowledge of the price variations among branded and generic medicines, an...
Overview on Study of consolidation parameters
drug development, IND, withdrawl of IND, exemption, IND review,
INVESTIGATIONAL NEW DRUG APPLICATION AS PER FEDERAL FOOD DRUG AND COSMETIC ACT
Dissolution is mass transfer process. Dissolution is mainly depend on aqueous solubility of drug. It...
The mission of the Clinical Trials Registry-India (CTRI) is to ensure that all clinical trials condu...
CLINICAL TRIAL REGISTRY OF INDIA
introduction to biosimilar drug difference between biosimilars and generic drugs global scenarios I...
optimization techniques and factorial designs in pharmaceutical product development.its examples in...
This presentation include basic introduction to pilot plant and scale up technology. following point...
ICH Guidelines were created by The International Council for Harmonization of Technical Requirements...
UPLC
IVIVC CORRELATION-INTRODUCTION-FUNDAMENTALS-LEVELS-METHOD DEVELOPMENT AND EVALUATION PREDICTABILITY-...
Objectives, Introduction, Advantages, Disadvantages, Principle, Instrumentation, Basic difference in...
Introduction Medicinal Chemistry
Pharmaceutical Product Development, Quality by Design and Process Development.
General pharmacology! Basics!
