Part-1। Pharmaceutical quality assurance 6th sem important questions। Short & long Questions।

Hey! My name is Shahruddin Khan Today In this video I provide Biopharmaceutics and pharmacokinetics 6th semester important questions with solution pdf. Watch Part-2 of Pharmaceutical quality assurance here 👇    • Video   Download pdf notes📝 of this video 📸 👇    • Pharmacy wala App Download Problem..!! 💥   Watch Important questions of other subjects of B Pharm 6th semester 👇🔥    • B Pharm 6th semester Important questions   Copyright disclaimer under section 107 of the copyright act 1976, allowance is made for ”fair use” for purposes such as critisism,comment ,news reporting , teaching,scholrship and research. Fair use is a use permitted by copyright statute that might otherwise be infringing. Non-profit, educational and personal use tips the balance in favor of fair use. Follow on Instagram:- (Personal)   / shahruddinkhan921   Follow on Instagram:- (Channel)   / pharmacy_wala   / Like Facebook Page :- https://www.facebook.com/profile.php?... ___________________________________________ Join Telegram channel link 👇 •●◉✿Pharmacy wala✿◉●• It is official telegram account of Pharmacy wala channel (shahruddin khan) Join this. https://t.me/pharmacywala15M Join whatsapp group👇 https://chat.whatsapp.com/ElxPp2Dt1a6... ____________________________________________ #biopharmaceutics #pharmacokinetics #pharmacology #medicinalchemistry #pharmacognosy #pharmaceutics #organicchemistry #importantquestions #bpharmacy #6thsemester #syllabus #importantquestions #exam Unit-I Quality Assurance and Quality Management concepts: Definition and concept of Quality control, Quality assurance and GMP. Total Quality Management (TQM): Definition, elements, philosophies. ICH Guidelines: purpose, participants, process of harmonization, Brief overview of QSEM, with special emphasis on Q-series guidelines, ICH stability testing guidelines. Quality by design (QbD): Definition, overview, elements of QbD program, tools. ISO 9000 & ISO14000: Overview, Benefits, Elements, steps for registration. NABL accreditation: Principles and procedures. Unit-II Organization and personnel: Personnel responsibilities, training, hygiene and personal records. Premises: Design, construction and plant layout, maintenance, sanitation, environmental control, utilities and maintenance of sterile areas, control of contamination. Equipments maintenance, purchase specifications and maintenance of stores for raw materials. and raw materials: Equipment selection, purchase specifications, Unit-III Quality Control: Quality control test for containers, rubber closures and secondary packing materials. Good Laboratory Practices: General Provisions, Organization and Personnel, Facilities, Equipment, Testing Facilities Operation, Test and Control Articles, Protocol for Conduct of a Nonclinical Laboratory Study, Records and Reports, Disqualification of Testing Facilities. Unit-IV Complaints: Complaints and evaluation of complaints, Handling of return good, recalling and waste disposal. Document maintenance in pharmaceutical industry: Batch Formula Record, Master Formula Record, SOP, Quality audit, Quality Review and Quality documentation, Reports and documents, distribution records. Unit-V Calibration and Validation: Introduction, definition and general principles of calibration, qualification and validation, importance and scope of validation, types of validation, validation master plan. Calibration of pH meter, Qualification of UV-Visible spectrophotometer, General principles of Analytical method Validation. Warehousing: Good warehousing practice, materials management.