gempex China Ltd.
CN
/
EN
gempex GmbH
DE
/
EN
400-166-2002
Company
Company Overview
Core Team
Mission Statement
Industry Resources
News
Services
Global Compliance
GMP Consultancy
GAP Analysis
Mock Inspection
GMP Training
GMP Inspection Support
3
rd
Party Audit
QP Inspection
Oversea Inspection
Facilities Compliance
New Plant C & Q
Design Review
Validation System Establishment
User Requirements Specification
Risk Management / Risk Analysis
Validation Master Plan
Facilities & Equipment Qualification
Processes Validation
Computerized System
CS Management System
CSV Computerized System Validation
Software Validation
Infrastructure Platform
Data Integrity (DI)
CS Compliance Training
Plant QMS
Structure Concept
QMS Establishment
Compliance Review
Continuous Monitoring
Integration & Optimization
Risk Management
Statistics Application
Routine quality Consulting
Multination MAH/MAA
Strategy Consulting
MAH/MAA QMS
License Application and Inspection
Outsourced QA
CMO/CDMO Management
GxP -GMP/GVP/GDP…
Cases
GMP Knowledge
Careers
Contact Us
Home
Company
Company Overview
Core Team
Mission Statement
Industry Resources
News
Services
Global Compliance
GMP Consultancy
GAP Analysis
Mock Inspection
GMP Training
GMP Inspection Support
3
rd
Party Audit
QP Inspection
Oversea Inspection
Facilities Compliance
New Plant C & Q
Design Review
Validation System Establishment
User Requirements Specification
Risk Management / Risk Analysis
Validation Master Plan
Facilities & Equipment Qualification
Processes Validation
Computerized System
CS Management System
CSV Computerized System Validation
Software Validation
Infrastructure Platform
Data Integrity (DI)
CS Compliance Training
Plant QMS
Structure Concept
QMS Establishment
Compliance Review
Continuous Monitoring
Integration & Optimization
Risk Management
Statistics Application
Routine quality Consulting
Multination MAH/MAA
Strategy Consulting
MAH/MAA QMS
License Application and Inspection
Outsourced QA
CMO/CDMO Management
GxP -GMP/GVP/GDP…
Cases
GMP Knowledge
Careers
Contact Us
gempex China Ltd.
CN
/
EN
gempex GmbH
DE
/
EN
About gempex
Company Overview
Core Team
Mission Statement
Industry Resources
News
About gempex
About gempex
GMP Knowledge
Technical Articles
Knowledge Sharing
On-line Courses
Free Manuals
Technical Articles
Qualification 4.0: Unused Opportunities-Part 2
Qualification 4.0: Unused Opportunities-Part 1
Basic Principles of an Effective and Efficient Qualification-Part 4
Basic Principles of an Effective and Efficient Qualification-Part 3
Basic Principles of an Effective and Efficient Qualification-Part 2
Basic Principles of an Effective and Efficient Qualification-Part 1
Basic Principles of Effective and Efficient Qualification Part 2
Basic Principles of Effective and Efficient Qualification Part 1
Cleaning Validation in the Production of Active Ingredients
How Suppliers Can Support Their Customers from Pharmaceutical Industries
More
Knowledge Sharing
Design Pharmaceutical Qualification Processes Efficiently
EU MDR - New Reporting and Documentation Requirements for Distributors and Importers of Medical Devices
ICH Q12 Pharmaceutical Product Lifecycle Management
Modern Qualification
On-line Courses
Internationalization of Chinese Pharmaceutical Enterprises
WebSeminar: EU MDR-Clinical Data
gempex WebSeminar Produktzulassung EU USA
Industry 4.0 meets Inspection Readiness
Free Manuals