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GB/T 28671-2012 in English

GB/T 28671-2012 in English

VALID

Guidelines for pharmaceutical machinery validation

  • Issued on:2012-09-03
  • Implemented on:2013-07-01
  • File Format:PDF
  • Delivery:Via email within 1~3 business days
Price(USD): $720.00
$699.00
Standard No: GB/T 28671-2012
Document status: VALID
Title in English: Guidelines for pharmaceutical machinery validation
Title in Chinese: 制药机械(设备)验证导则
Language: English
File Format: Electronic (PDF)
Delivery: Via email within 1~3 business days
Issued on: 2012-09-03
Implemented on: 2013-07-01
ICS Classification: 11.120-Pharmaceutics
Chinese Classification: C90-Pharmaceutical, safety machinery and tool in general
Professional Classification: GB-National Standard
Related Keywords: pharmaceutical machinery
pharmaceutical machinery validation scopethis standard
pharmaceutical equipment
verification purposes
verification work
Related Topics: pharmaceutical
Equipment
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device verification
pharmaceutical technology
Analytical Equipment Validation
pharmaceutical equipment
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Drug Internal Validation
Mechanical Verification System
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Xishuang pharmaceutical equipment
Production Equipment Verification
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Protocol Pharmacy
Pharmaceutical Equipment Manufacturing
Pharmacokinetic verification
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Pharmaceuticals and Manufacturing
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new pharmaceutical equipment
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How to verify the device
Biopharmaceutical Device Validation
Equipment acceptance machinery
Device Sameness Verification
Equipment Year Verification
Drug verification
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Domestic new pharmaceutical equipment
drug verification batch
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Verification scope
Mechanical experiment equipment
Class I equipment verification
GBT28671
Mechanical Validation Kit
Medical Methodology Validation
Pharmacopoeia Methodology Validation
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Methodological Validation Pharmacopoeia
Pharmacopoeia Methodology Validation
verify

《GB/T 28671-2012制药机械(设备)验证导则》由TC356(全国制药装备标准化技术委员会)归口,主管部门为国家标准化管理委员会。


Scope

This standard specifies the terms and definitions, verification purposes, principles, procedures and schemes for pharmaceutical machinery (equipment) (hereinafter referred to as pharmaceutical equipment) verification. This standard is applicable to guide the verification work of design verification, installation verification, operation verification and performance verification of pharmaceutical equipment.

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