astm e2500

2
ASTM E2500 http://www.leanvalidation.eu/lean-validation/astm-e2500[6/23/2013 9:17:56 PM] Home Lean Validation ASTM E2500 ASTM E2500 ASTM E2500-7 is a consensus guide with legal reference and global impact. The has Copyright by ASTM Int'l (all rights reserved) and can be purchased at www.astm.org. The ASTM E2500 has a lean approach for validation and is in line with FDA’s Pharmaceutical cGMP's for the 21st century, EMEA, GAMP 5 and ICH Q8 and Q9. Add new comment Approach The guide allows flexibility in changes before final acceptance of the system. The level of detail for documentation is based on risk in relation to patient safety and product quality. Before acceptance of the system the design and implementation is done under Good Engineering Practice (GEP) by Subject Matter Experts (SME); after acceptance GMP related changes are managed and approved by QA. Add new comment Key concepts The following key concepts are mentioned in the guide: Add new comment Risk-based Approach Science-based Approach Critical Aspects of Manufacturing Systems Quality by Design Good Engineering Practice Subject Matter Expert Use of Vendor Documentation Continuous Process Improvement The validation process Process The validation process is divided into the following sections Requirements definition Specification and design Verification Acceptance and release Home Lean Validation Validation Lean Manufacturing Six Sigma Project Management ISA Standards APC News Contact Top of page

Upload: madosb5133

Post on 09-Feb-2016

299 views

Category:

Documents


0 download

TRANSCRIPT

Page 1: Astm e2500

ASTM E2500

http://www.leanvalidation.eu/lean-validation/astm-e2500[6/23/2013 9:17:56 PM]

Home Lean Validation ASTM E2500

ASTM E2500

ASTM E2500-7 is a consensus guide with legal reference and global impact. The has Copyright by ASTM Int'l (all rights reserved) and can be purchased at www.astm.org.

The ASTM E2500 has a lean approach for validation and is in line with FDA’s Pharmaceutical cGMP's for the 21st century, EMEA, GAMP 5 and ICH Q8 and Q9.

Add new comment

ApproachThe guide allows flexibility in changes before final acceptance of the system. The level of detail for documentation is based on risk in relation to patient safety and product quality. Beforeacceptance of the system the design and implementation is done under Good Engineering Practice (GEP) by Subject Matter Experts (SME); after acceptance GMP related changes aremanaged and approved by QA.

Add new comment

Key conceptsThe following key concepts are mentioned in the guide:

Add new comment

Risk-based ApproachScience-based ApproachCritical Aspects of Manufacturing SystemsQuality by DesignGood Engineering PracticeSubject Matter ExpertUse of Vendor DocumentationContinuous Process Improvement

The validation process

ProcessThe validation process is divided into the following sections

Requirements definitionSpecification and designVerificationAcceptance and release

Home Lean Validation Validation Lean Manufacturing Six Sigma Project Management ISA Standards APC News Contact

Top of page

Page 2: Astm e2500

ASTM E2500

http://www.leanvalidation.eu/lean-validation/astm-e2500[6/23/2013 9:17:56 PM]

Joomla template created with Artisteer by René van Opstal.

Add new comment

The supporting processesThe supporting processes support the validation during the whole process.

Add new comment

risk managementdesign reviewchange management

DifferencesThe differences betwee the ASTM guide and the ISPE Baseline guide are shown in the table below.

ISPE Baseline guide ASTM guide

Add new comment

Design inputsImpact assessmentDesign QualificationCommissioningMultiple trial runs to get things rightIQ, OQ, PQ and acceptance criteriaGEP Scope and QA ScopeoverlappedFocused on DocumentationDeliverablesRigid Change Management

Design inputsDesign ReviewRisk MitigationCritical Control Parameters define Acceptance CriteriaVerification TestingPerformance TestingGEP Scope and QA Scope have clear boundaryProcess, Product Quality and Patient SafetyQuality by Design, Design Space and ContinuousImprovement

Copyright © 2010 ---.All Rights Reserved.