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Bpharmacy 8 semester pharmaceutical Regulatory science bp804T Unit I New Drug Discovery and develo...
B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY SCIENCE (Theory). Unit-I Chapter...
Pharmacovigilance, the science of monitoring and evaluating the safety of medicines, relies on a rob...
Biopharmaceutics Lecture 1 Instructor: Baasir Umair Khattak (MPhil Pharmacology, QAU) Topic: The Em...
The science of dosage or posology (from Greek posos, how much, and logos, study) is a branch of phar...
Drug action refers to the specific biochemical interactions between a substance (drug) and its targe...
This presentation delves into the systemic blind spots within pharmaceutical science and regulatory ...
Pharmacovigilance, derived from the Greek words "pharmakon" (drug) and "vigilare"...
The Central Drugs Standard Control Organization (CDSCO) is India's national regulatory body for ...
Pharmacovigilance refers to the science and activities related to the detection, assessment, underst...
drug development, IND, withdrawl of IND, exemption, IND review,
The Food and Drug Administration (FDA) stands as an essential institution in our modern world, ensur...
Pharmacovigilance is the science and activities related to the detection, assessment, understanding,...
An Individual Case Safety Report (ICSR) is a document that contains information about a single adver...
Causality assessment is the process of evaluating the relationship between a medical event, such as ...
India’s bioanalytical testing services market is witnessing rapid growth, supported by strong gove...
Different organization of US FDA and its responsibility.
USFDA
ICH Guideline Q8 Pharmaceutical Development
Regulation For Combination of products & medical devices
The pharmaceutical Quantity by Design (QbD) is a systemic approach to development that begins with p...
its about the regulatory agencies all over the world
QbD can be applied to the development and evaluation of analytical methods. During method developmen...
UNIT 5 RA 1ST SEM
