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ask about validation一些很有用的pdf文章
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4 Steps to Risk Analysis & Management.pdf
411.8 KB, 下载次数: 77
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7 Items to Consider When Implementing Backup and Restore Policies.pdf
395.54 KB, 下载次数: 66
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9 Essential IT SOP’s When Implementing a Regulated Computer System.pdf
970.15 KB, 下载次数: 77
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9 Things to Consider with CSV Periodic Reviews.pdf
778.5 KB, 下载次数: 87
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10 Things To Consider When It Comes To Qualifying Autoclaves.pdf
792.25 KB, 下载次数: 74
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12 Common Audit Findings Associated with Equipment Qualifications.pdf
387.84 KB, 下载次数: 74
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17 Questions You Need to Ask a Software Vendor About their Quality System.pdf
433.11 KB, 下载次数: 69
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21 CFR Part 11 – System Access to Authorized Individuals.pdf
357.96 KB, 下载次数: 71
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21 CFR Part 11 & Analytical Equipment Interfaced to a Computer.pdf
317.87 KB, 下载次数: 67
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21 CFR Part 11 A Dummies Guide Part 1 – Sec. 11.1 Scope.pdf
835.45 KB, 下载次数: 73
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21 CFR Part 11 A Dummies Guide Part 2 – Sec. 11.2 Implementation.pdf
616.69 KB, 下载次数: 69
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21 CFR Part 11 A Dummies Guide Part 3 – Sec. 11.3 Definitions.pdf
844.58 KB, 下载次数: 70
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A Risk Based, Pragmatic Approach to Alarm Management in Regulated Environments.pdf
390.5 KB, 下载次数: 73
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A Risk-Based Approach to Validation – Overview.pdf
1.5 MB, 下载次数: 83
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A Simple Approach to Stability Chamber Qualification-1.pdf
328.47 KB, 下载次数: 67
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Agents For Cleaning Validation – Alkaline Vs Acidic.pdf
489.54 KB, 下载次数: 72
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Airlocks –The Ventricles of Cleanroom.pdf
327.46 KB, 下载次数: 68
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An Easy Way to Validate a SQL Report.pdf
518.59 KB, 下载次数: 65
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Analytical Instrument Qualification and System Validation.pdf
686.28 KB, 下载次数: 76
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ASTM E2537 – Standard Guide for Application of Continuous Quality Verification.pdf
891.3 KB, 下载次数: 79
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Audit Trails and the Meaning of Independent.pdf
496.33 KB, 下载次数: 72
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Blend Uniformity in Pharmaceutical Solid Dosage Forms.pdf
371.57 KB, 下载次数: 79
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Challenges in Pharmaceutical Product Life Cycle Management.pdf
1.24 MB, 下载次数: 75
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Cleaning In Place (CIP) Vs Cleaning Out of Place (COP).pdf
214.15 KB, 下载次数: 70
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Cleaning Validation Acceptance Criterion.pdf
287.12 KB, 下载次数: 70
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Cleaning Validation Mechanism’s – The Top Four!.pdf
625.91 KB, 下载次数: 63
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Cleaning Validation Methods.pdf
535.43 KB, 下载次数: 65
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Common Mistakes Made in Software Validation Operational Qualifications (OQ)-1.pdf
324.48 KB, 下载次数: 65
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Common Problems Associated With Validation.pdf
390.34 KB, 下载次数: 66
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Computer System Validation – Periodic Review.pdf
284.33 KB, 下载次数: 67
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Concepts Of Industrial Manufacturing Techniques.pdf
1.1 MB, 下载次数: 62
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COTS Software – 5 Essential Items to Consider.pdf
654.7 KB, 下载次数: 66
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Critical Parameters Affecting Process Validation.pdf
325.01 KB, 下载次数: 69
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Defining Calibration & Qualification of Equipment.pdf
320.71 KB, 下载次数: 62
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Disaster Recovery & Business Continuity – Did You Validate.pdf
1.56 MB, 下载次数: 73
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Do You Dry Run Your Test Scripts.pdf
294.28 KB, 下载次数: 68
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Do you Follow a Full Lifecycle When Performing Validation Projects.pdf
292.46 KB, 下载次数: 68
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Document Management Systems (EDMS) in the Cloud-What You Need to Know.pdf
1.18 MB, 下载次数: 73
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Document Retention-Regulatory Guidance.pdf
331.95 KB, 下载次数: 66
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Documents Recommended for GxP Software Implementation.pdf
774.94 KB, 下载次数: 64
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Efficient Software Testing for a Regulated Environment.pdf
492.25 KB, 下载次数: 70
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Electronic Records – CSV FDA Warning Letters.pdf
613.22 KB, 下载次数: 70
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Engineering with an S88 Approach-Part 2.pdf
1.01 MB, 下载次数: 73
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Engineering with an S88 Approach-Part 3.pdf
331.18 KB, 下载次数: 65
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Equipment Installation Qualification – What Should Be In Your Protocol.pdf
301.5 KB, 下载次数: 67
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Equipment Validation – Where Do I Start.pdf
384.78 KB, 下载次数: 66
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EU Annex 11 – Computer System Inventory.pdf
847.2 KB, 下载次数: 67
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Eudralex Volume 4, Annex 11 – A Refresher!.pdf
30.26 KB, 下载次数: 53
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Event Driven and Time Driven CSV Revalidation.pdf
691.64 KB, 下载次数: 68
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Five Questions You Need to Ask When Designing a HVAC System.pdf
348.65 KB, 下载次数: 65
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Generating Retrospective Specifications When URS’s Don’t Exist.pdf
263.58 KB, 下载次数: 68
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Good Documentation Practices (GDP) are Critical to Success!.pdf
775.27 KB, 下载次数: 67
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How to Create a Bullet-Proof User Requirement Specification (URS).pdf
1.02 MB, 下载次数: 70
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How to Deploy a Software Application in a GxP Environment – Planning & Design.pdf
1.21 MB, 下载次数: 64
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How to Design a Clean Room in a Regulated Facility.pdf
937.45 KB, 下载次数: 68
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How to Write an Effective Cleaning Procedure.pdf
284.21 KB, 下载次数: 62
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How We Contaminate Clean Rooms.pdf
336.12 KB, 下载次数: 65
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Internal Audits – Good Practice for 2010!.pdf
293.65 KB, 下载次数: 67
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Lifecycle Documentation – Deliverable Errors.pdf
598.2 KB, 下载次数: 70
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LIMS Supplier Audits & Design Specifications.pdf
928.24 KB, 下载次数: 79
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Managing Requirements Throughout Multiple Life Cycle Stages.pdf
975.3 KB, 下载次数: 74
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Managing the Risks of the Regulated Cloud.pdf
2.35 MB, 下载次数: 74
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Manufacturing Engineering Systems And The Challenges.pdf
985.97 KB, 下载次数: 70
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Manufacturing Execution Systems (MES) & Validation.pdf
310.57 KB, 下载次数: 63
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Measuring, Controlling and Predicting Process Performance.pdf
30.26 KB, 下载次数: 53
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MS Access Validation – Top Tips.pdf
1.62 MB, 下载次数: 71
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New Forum – Good Automated Manufacturing Practice GAMP 5.pdf
500.92 KB, 下载次数: 63
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No Longer 3 Golden Batches, So Just How Many Process Performance Qualification B.pdf
435.13 KB, 下载次数: 73
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Operational Excellence and Process Evaluation In Pharmaceutical Manufacturing.pdf
883.21 KB, 下载次数: 71
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Out Of Trend Results – OOT’s.pdf
311.19 KB, 下载次数: 71
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Packaging Validation – A Simple Example.pdf
299.57 KB, 下载次数: 67
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Paperless Manufacturing – The Easy to Implement Cost Effective Way!.pdf
444.13 KB, 下载次数: 66
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Paperless Validation has arrived for the Life Science Industry.pdf
485.84 KB, 下载次数: 72
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Part-11-Sample.pdf
2.6 MB, 下载次数: 79
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Personnel Qualification in Aseptic Areas.pdf
1.1 MB, 下载次数: 81
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Pharmaceutical “Quality by Design” (QbD)-An Introduction, Process Development .pdf
453.81 KB, 下载次数: 66
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Pharmaceutical Equipment Management.pdf
272.52 KB, 下载次数: 69
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Pharmaceutical Excipient Factors Affecting Tablet Formulation And Regulatory Req.pdf
285.98 KB, 下载次数: 67
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Pre-Execution Approval of Validation Test Scripts – What To Look Out For!.pdf
336.44 KB, 下载次数: 66
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Prevention and Control of Microbial Contamination For Pharmaceutical Products.pdf
758.97 KB, 下载次数: 71
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Prevention Of Contamination And Cross -Contamination In Pharmaceutical Dosage Forms.pdf
1.05 MB, 下载次数: 70
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Process Control Systems GAMP 5 Software Categories.pdf
411.78 KB, 下载次数: 67
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Process Validation 1987 Vs 2011 – What You Need To Know!.pdf
457.45 KB, 下载次数: 78
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Product Selection Criteria for Retrospective Validation.pdf
271.77 KB, 下载次数: 64
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Qualification of Air Handling Systems.pdf
31.55 KB, 下载次数: 58
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Qualification of Air Handling Systems1.pdf
286.9 KB, 下载次数: 66
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Quality Risk Management within the Pharmaceutical Industry.pdf
1.09 MB, 下载次数: 78
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Quality Vs Validation – Protocol Acceptance Criteria.pdf
351.54 KB, 下载次数: 64
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Reducing Validation Time and Cost-How GAMP & Risk Based Approaches are Reducin.pdf
354.55 KB, 下载次数: 65
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Risk Assessment in Cleaning Validation – An Overview.pdf
708.15 KB, 下载次数: 71
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Risk Based Approach to Reduce Costs when Implementing Regulated Software.pdf
987.44 KB, 下载次数: 69
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S88 – A New Approach to Engineering- Part 1.pdf
785.42 KB, 下载次数: 65
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Saturated Steam – Efficient Sterilization.pdf
1.32 MB, 下载次数: 72
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Showing Insufficient Deviations to Support Comprehensive Testing.pdf
382.61 KB, 下载次数: 65
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Software Master Validation Plan All You Need to Know!.pdf
929.66 KB, 下载次数: 72
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Software Patches and Validated Applications.pdf
574.81 KB, 下载次数: 64
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Software Validation in a Nutshell! The 5 Minute Guide to Understanding the Principles.pdf
352.24 KB, 下载次数: 66
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Software Validation Security Testing – 12 Items to Consider.pdf
336.75 KB, 下载次数: 68
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Software Vendor Supplier Audit – Top Tips.pdf
613.33 KB, 下载次数: 66
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Software-Validation-Book.pdf
1.81 MB, 下载次数: 75
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Spreadsheet or Excel Validation, There is No Risk!.pdf
1004.65 KB, 下载次数: 71
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Technology Trends Facing Life Sciences in 2013.pdf
1.09 MB, 下载次数: 67
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Test Method Validation – The Starting Point.pdf
361.3 KB, 下载次数: 63
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The 3 Steps to Awesome Design Qualifications.pdf
557.33 KB, 下载次数: 72
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The Application of FMEA to Laboratory Instrument Qualification Risk Management .pdf
1.08 MB, 下载次数: 73
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The Application of FMEA to Laboratory Instrument Qualification Risk Management .pdf
1.88 MB, 下载次数: 89
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The Concept of Air Handling System Validation.pdf
535.9 KB, 下载次数: 71
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The Difference Between a FAT and a SAT.pdf
394.82 KB, 下载次数: 71
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The Foundations for a Solid CSV Validation Effort.pdf
843.21 KB, 下载次数: 75
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The Four Types of Process Validation.pdf
364.34 KB, 下载次数: 64
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The Great Screenshot Debate – Vote Now!.pdf
393.24 KB, 下载次数: 67
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The Qualified Person (QP) and Validation.pdf
378.34 KB, 下载次数: 65
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The Relationship between IQ, OQ, FATs and SATs.pdf
107.63 KB, 下载次数: 65
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Thermal Validation-Measure Right for your Range.pdf
1.33 MB, 下载次数: 71
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Things You Need to Consider When Recording Results in Validation Protocols.pdf
295.05 KB, 下载次数: 67
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To Sign or Not to Sign – That is the Question!.pdf
655.3 KB, 下载次数: 67
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Top 6 Tips When Implemen... askaboutValidation.pdf
30.04 KB, 下载次数: 55
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Top 6 Tips When Implementing a Regulated Software Application.pdf
290.29 KB, 下载次数: 66
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Top 10 Concerns Associated with Clinical Trials.pdf
1.02 MB, 下载次数: 73
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Top 10 Questions Concerning IT Data Integrity.pdf
325.26 KB, 下载次数: 64
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Top 12 Audit Findings for Equipment Systems within a Regulated Environment.pdf
405.69 KB, 下载次数: 69
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Top 22 Reasons Why Risk Assessments are So Difficult.pdf
352.95 KB, 下载次数: 71
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Top Tips for Cleaning Method Development.pdf
270.13 KB, 下载次数: 66
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Top Tips for Organic Solvent Cleaning.pdf
221.44 KB, 下载次数: 69
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Top Tips for Pharmaceutical Automation and Validation.pdf
294.59 KB, 下载次数: 64
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Top Tips for Protocol Execution.pdf
935.47 KB, 下载次数: 65
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Top Tips On How to Calibrate a Thermo Hygrometer.pdf
671.4 KB, 下载次数: 62
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Top Tips On How To Investigate Laboratory & Manfacturing Sterility Failures.pdf
643.45 KB, 下载次数: 60
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Top Tips When Auditing a Water Purification Treatment Supplier.pdf
570.57 KB, 下载次数: 62
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Top Tips When Creating a URS for a Purified Water System.pdf
866.08 KB, 下载次数: 68
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Typical Contents of a Validation Master Plan (VMP).pdf
87.78 KB, 下载次数: 60
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Validating Excel Spreadsheets and Automated Forms.pdf
1.06 MB, 下载次数: 71
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Validating SharePoint-6 Steps to Take Before You Start.pdf
502.15 KB, 下载次数: 67
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Validating The Cloud – Top 25 Questions You Need To Ask!.pdf
464.06 KB, 下载次数: 70
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Validation Deviations – An Important Part of Any Validation Project.pdf
303.16 KB, 下载次数: 66
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Validation Master Plans Vs Project Validation Plans.pdf
276.56 KB, 下载次数: 70
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Validation of MS Excel Spreadsheets.pdf
366.25 KB, 下载次数: 74
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Validation of Water Systems.pdf
449.7 KB, 下载次数: 70
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Validation Protocol Execution Tips – Top 10.pdf
410.79 KB, 下载次数: 66
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Validation Stages and SOP’s.pdf
449.65 KB, 下载次数: 69
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Validation Templates – The Starting Point of a Successful Validation Project.pdf
387.61 KB, 下载次数: 75
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Vendor Audits – Top Tips.pdf
366 KB, 下载次数: 67
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Warehousing Mapping a Brief Guide to Success.pdf
377.2 KB, 下载次数: 72
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What is Metadata and it’s GxP Regulatory Impact.pdf
665.84 KB, 下载次数: 70
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Why Validation is Important!.pdf
288.13 KB, 下载次数: 77
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Why Validation Projects Take So Long – Paperwork!.pdf
311.48 KB, 下载次数: 66
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Wireless Vs Wired Networks In a Regulated Environment.pdf
658.48 KB, 下载次数: 79
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