Tools to Implement QBD – Quality Assurance | B.Pharmacy 6th Semester Design of experiments (DOE) Risk Assessment Process Analytical Technology Quick Download
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Methods of analytical validation – Quality Assurance | B.Pharmacy 6th Semester Quick Download
Methods of analytical validation – Quality Assurance – B.Pharmacy 6th Semester Read More »
Presentation on GMP | Quality Assurance | B.Pharmacy 6th Semester Quick Download Good Manufacturing Practice is a set of regulations , codes and guidelines for the manufacture of drug substances and drug products , medical devices and foods. Good Manufacturing Practices are regulations that describe the methods, equipment, facilities, and controls. HK Technical PGIMS –
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NATIONAL ACCREDITATION BOARD FOR TESTING & CALIBRATIONLABORATORIES (NABL) NATIONAL ACCREDITATION BOARD FOR TESTING & CALIBRATIONLABORATORIES (NABL) National Accreditation Board for Testing and Calibration Laboratories (NABL) is the sole Laboratory Accreditation body authorised by Government of India (COD). NABL is an autonomous body under the aegis of Department of Science & Technology (COD). NABL
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Calibration of pH Meter in Quality Assurance B.Pharmacy 6th Semester CALIBRATION OF pH METERB.PHARMACY 6TH SEMESTER INTRODUCTION A pH meter is an electronic instrument used for measuring the pH (acidity or alkalinity) of a liquid (though special probes are sometimes used to measure the pH of semi-solid substances). A typical pH meter consists of
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Write a Note on Requirements for residual solvents in pharmaceutical products. RESIDUAL SOLVENTS UNDER USP 467 (ICH Q3C) GUIDELINES Residual solvents in pharmaceuticals are defined by the ICH as organic volatile chemicals that are used or produced in the manufacture of drug substances, excipients, or in the preparation of drug products. In general, solvents are
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Question: Write a short note on Conduct of a non-clinical laboratory studies. [Quality Assurance in Pharmacy] Answer: Read here: Protocol for non-clinical studies Conduct of a non-clinical laboratory studies: The nonclinical laboratory study shall be conducted in accordance with the protocol. The test systems shall be monitored in conformity with the protocol. Specimens shall be identified
Question: Write a short note on protocol for non-clinical studies. [Quality Assurance in Pharmacy] Answer: PROTOCOL FOR NON-CLINICAL STUDIES: Each study shall have an approved written protocol that clearly indicates the objectives and all methods for the conduct of the study. The protocol shall contain, as applicable, the following information: A descriptive title and statement