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FDA 21 CFR Part 820 vs. ISO 13485:2016 vs. ISO 13485:2003

FDA 21 CFR Part 820 vs. ISO 13485:2016 vs. ISO 13485:2003

2009年1月1日

greenlight.guru

Your 1 Minute Guide to Incoming Material Inspection – 21 CFR Part 820.80(b) [Video] - LearnGxP: Accredited Online Life Science Training Courses

Your 1 Minute Guide to Incoming Material Inspection – 21 CFR Part 820.80(b) [Video] - LearnGxP: Accredited Online Life Science Training Courses

2021年9月26日

21 CFR Part 820 Subpart G – Production and Process Controls - LearnGxP: Accredited Online Life Science Training Courses

21 CFR Part 820 Subpart G – Production and Process Controls - LearnGxP: Accredited Online Life Science Training Courses

2021年9月23日

US FDA 21 CFR 820.30 (Design Controls For Medical Devices) | Operon Strategist

US FDA 21 CFR 820.30 (Design Controls For Medical Devices) | Operon Strategist

2022年6月3日

operonstrategist.com

[Hot Item] Inscinstech Protein Purification System (Unique AutoPure100-M402) Fplc Can Meet The Requirements of FDA 21 CFR Part 11/GLP/GMP

[Hot Item] Inscinstech Protein Purification System (Unique AutoPure100-M402) Fplc Can Meet The Requirements of FDA 21 CFR Part 11/GLP/GMP

made-in-china.com

[Hot Item] Inscinstech Protein Purification System (Unique AutoPure150-M804) Fplc Can Meet The Requirements of FDA 21 CFR Part 11/GLP/GMP

[Hot Item] Inscinstech Protein Purification System (Unique AutoPure150-M804) Fplc Can Meet The Requirements of FDA 21 CFR Part 11/GLP/GMP

made-in-china.com

[Hot Item] Inscinstech Protein Purification System (Unique AutoPure150-M402) Fplc Can Meet The Requirements of FDA 21 CFR Part 11/GLP/GMP

[Hot Item] Inscinstech Protein Purification System (Unique AutoPure150-M402) Fplc Can Meet The Requirements of FDA 21 CFR Part 11/GLP/GMP

made-in-china.com

[Hot Item] Inscinstech Protein Purification System Lab Instrument (Unique AutoPure100-L2) Fplc Can Meet The Requirements of FDA 21 CFR Part 11/GLP/GMP

made-in-china.com

[Hot Item] Sistema de purificación de proteínas Inscinstech (única AutoPure100-M402) Fplc puede satisfacer las necesidades de la FDA 21 CFR Parte 11/GLP/GMP

made-in-china.com

[Hot Item] Inscinstech Protein Purification System (Unique AutoPure150-M604) Fplc Can Meet The Requirements of FDA 21 CFR Part 11/GLP/GMP

made-in-china.com

[Hot Item] Sistema de purificación de proteínas de cromatografía iónica Inscinstech (UNIQUE AutoPure25-M402) El FPLC puede cumplir los requisitos de la parte 21 CFR de la FDA 11/GLP/GMP

made-in-china.com

Your 1 Minute Guide to Line Clearance in a GMP Production Environment [Video] - LearnGxP: Accredited Online Life Science Training Courses

2021年9月26日

Medical Device Product Identification - Part Numbering (820.60) [Video] - LearnGxP: Accredited Online Life Science Training Courses

2021年9月26日

GxP Training : #1 Certified Online Courses Provider for Life Sciences Professionals on LinkedIn: New Certified Training: 21 CFR Part 58 GLP: Good Laboratory Practice for…

FDA 21 CFR Part 820: 8 Most Common Mistakes to Avoid

2019年6月24日

greenlight.guru

Optimizing Quality Control Electronic Records for 21 CFR Part 11 Compliance

21 CFR Part 11: A Guide To FDA's Requirements

2018年9月11日

greenlight.guru

Your 2 Minute Guide to Specification, Alert and Action Limits – 820.70(a) [Video] - LearnGxP: Accredited Online Life Science Training Courses

2021年9月26日

A comprehensive review of the best 21 CFR Part 11 software in 2024

已浏览 2 次2019年6月2日

Campos de Batalha de Hearthstone terão confrontos em duplas a partir de 16 de abril

FDA QMSR Training USA | 21 CFR Part 820 and ISO 13485 Course

GMP Detox 21 CFR Part 820 Medical Devices - Short Introduction

YouTubeGMP Detox

What is the difference between the new QMSR and 21 cfr part 820?

已浏览 10 次6 个月之前

YouTubePathWise

FDA Aligning to ISO 13485:2016 (and Why It Matters)

2018年10月8日

greenlight.guru

Medical Device Manufacturers compliant to FDA need to take actions soon!

已浏览 7 次4 个月之前

YouTubeKristine Witzel, Quality Management Consulting

Format & Content of a Medical Device File (MDF) - ISO 13485:2016, Clause 4.2.3

已浏览 621 次9 个月之前

YouTubeMedical Device Academy

Integrity Manager, module logiciel pour travailler selon les recos de la norme FDA CFR 21 Part 11

已浏览 8 次1 个月前

YouTubeMicrovision Instruments

We prioritize Quality at Proterial HPMS.

已浏览 103 次2023年11月21日

YouTubeProterial Cable America, Inc.

Understanding 21 CFR Part 210: An Essential Guide to GMP Compliance for the Pharmaceutical Industry

已浏览 96 次1 个月前

YouTubePharma Capital

21 CFR 820 75 Process Validation Concepts

已浏览 257 次2023年7月31日

YouTubePharma World K

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