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050 4 _aRS400-431
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072 7 _aSCI013040
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072 7 _aPNB
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245 1 0 _aModern Aspects of Pharmaceutical Quality Assurance
_h[electronic resource] :
_bDeveloping & Proposing Application models, SOPs, practical audit systems for Pharma Industry /
_cedited by Minal Ghante, Manohar Potdar, Vidhya Bhusari.
250 _a1st ed. 2024.
264 1 _aSingapore :
_bSpringer Nature Singapore :
_bImprint: Springer,
_c2024.
300 _aVIII, 523 p. 1 illus.
_bonline resource.
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bc
_2rdamedia
338 _aonline resource
_bcr
_2rdacarrier
347 _atext file
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505 0 _aChater 1 Introduction: Quality Assurance from Perspective of Pharmaceutical Industry -- Chapter 2 Six-sigma Model in Pharma Industry (Part-I) -- Chapter 3. Six-sigma Model in Pharma Industry (Part-II) -- Chapter 4 Developing a practical audit system for a pharmaceutical industry based on six system inspection model -- Chapter 5 -- Compliance Tools to Assist the Drug Industry for Regulatory Audits from Developed Countries -- Chapter 6 Developing an Application Model for Planning, Controlling, Improving and Assuring Quality for Pharmaceutical Industry - covering Quality Planning and Quality Control -- Chapter 7 Developing an Application model for Improving Quality for Pharmaceutical Manufacturing based on the Quality principle- covering Quality Improvement and Quality Assurance Audit -- Chapter 8 Developing a Design Qualification Protocol as Standard Operating Procedure for a Pharmaceutical Plant Facility Meeting cGMP requirement for Tablets andCapsule Manufacturing Department -- Chapter 9 Developing a Design Qualification Protocol as Standard Operating Procedure for a Pharmaceutical Plant Facility Meeting cGMP requirement for Liquid oral and Ointment Department -- Chapter 10 Developing a simplified model Standard Operating Procedure to implement quality metrics for Pharmaceutical Manufacturing System -- Chapter 11 Documentation and data integrity in Pharmaceutical Industry -- Chapter 12 Quality Risk Management. Chapter 13 Deviation, Change control and CAPA.
520 _aThe pharmaceutical quality system ensures that the process performance is suitably achieved, the product quality is regularly met, improved opportunities are identified and evaluated, and the knowledge is constantly expanded. Auditing also plays a crucial role within the pharmaceutical industry. It helps to assess and review quality to improve and build a better system for the benefit of companies. This book aims to develop a tool that will substantially decrease the number of Inspectional Observations and Warning letters, thus eliminating Import Alerts and Consent Decree. This book targets the Pharmaceutical Industry and students of Pharmaceutical Quality Assurance so they can get in hand-ready consolidated information on Pharmaceutical Quality guidelines, Quality metrics, and implementation of simplified SOP guidelines, plant layouts to implement Quality metrics for Pharmaceutical Manufacturing systems in tablets, capsules, liquid orals, and semi-solid dosage forms. The chapters cover the various aspects of Pharmaceutical Quality Assurance. The selection of topics is mainly based on the requirements of Pharmaceutical regulatory guidelines of India, the UK, the USA, Australia, and South Africa. Each chapter includes the abstract, detailed explanation, implementation guidelines, flowcharts, layouts, and Standard Operating Procedure of quality metrics for the Pharmaceutical Manufacturing System.
650 0 _aPharmaceutical chemistry.
_967843
650 0 _aIndustrial policy.
_969808
650 0 _aDrug delivery systems.
650 1 4 _aPharmaceutics.
_967846
650 2 4 _aRegulation and Industrial Policy.
_969809
650 2 4 _aDrug Delivery.
_969429
700 1 _aGhante, Minal.
_eeditor.
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_4http://id.loc.gov/vocabulary/relators/edt
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700 1 _aPotdar, Manohar.
_eeditor.
_4edt
_4http://id.loc.gov/vocabulary/relators/edt
_972792
700 1 _aBhusari, Vidhya.
_eeditor.
_4edt
_4http://id.loc.gov/vocabulary/relators/edt
_972793
710 2 _aSpringerLink (Online service)
773 0 _tSpringer Nature eBook
776 0 8 _iPrinted edition:
_z9789819992706
776 0 8 _iPrinted edition:
_z9789819992720
776 0 8 _iPrinted edition:
_z9789819992737
856 4 0 _uhttps://doi.org/10.1007/978-981-99-9271-3
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