QA, QC & GMP

• Training course on Quality Risk Management (QRM)
  Emne: QA, QC & GMP, QA, Risk management, Risk / failure investigations, Risk management
  Udbyder: DIA
  Sted: Copenhagen, Denmark
  Dato: 25 March 2012
  
• 1st CMC Forum in Japan: Challenges for Quality Improvement in Asia
  Emne: QA, QC & GMP, QA, GMP, Product development, CMC, Supply/distribution chain, Management
  Udbyder: DIA
  Sted: Tokyo, Japan
  Dato: 11 June 2012
  
• Quality by Design (QbD) in Pharmaceutical Development
  Emne: QA, QC & GMP, QA, Quality by design
  Udbyder: KU, FARMA
  Sted: Copenhagen, Denmark
  Dato: 13-17 August 2012
  
• DIA Practical GCP Compliance Auditing of Trials and Systems Training Course
  Emne: QA, QC & GMP, Audit-inspection, GCP, Clinical trials, Practice
  Udbyder: DIA
  Sted: London, England
  Dato: 17-19 October 2012
  

Courses from other providers

• BK/BKP52 - Accreditation of Laboratories for Technical Measurements
  Emne: QA, QC & GMP, Laboratories, GLP
  Udbyder: Syddansk Universitet
  Sted: Odense, Denmark
  Dato: A one semester course, running Spring and Autumn semesters
  
• PHARMACEUTICAL PACKAGING AND LABELLING ~ 2 Day WEBCAST
  Emne: QA, QC & GMP, Trial supply, Packaging, Packaging material, QC, QA
  Udbyder: Management FORUM
  Sted: Internet
  Dato: Any time
  
• Auditing Techniques for Clinical Research Professionals
  Emne: QA, QC & GMP, Audit-inspection, GCP, Clinical trials, Practice, Computer systems
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 6-7 February 2012
  
• Observation and Recording for Auditors
  Emne: QA, QC & GMP, Audit-inspection, Psychology, Practice, Strategy
  Udbyder: BARQA
  Sted: Cambridge, England
  Dato: 13-14 February 2012
  
• Good Manufacturing Practice in Pharmaceutical Laboratories
  Emne: QA, QC & GMP, Laboratories, GLP, GMP, GMP, Laboratories
  Udbyder: BARQA
  Sted: Cambridge, England
  Dato: 14 February 2012
  
• Validation of Molecular Biological Methods
  Emne: QA, QC & GMP, Biotech, Validation, Biotech, Process validation
  Udbyder: ECA
  Sted: Prague, Czech Republic
  Dato: 14-15 February 2012
  
• Audit Analysis and Reporting
  Emne: QA, QC & GMP, Audit-inspection, Management, Practice
  Udbyder: BARQA
  Sted: Cambridge, England
  Dato: 16-17 February 2012
  
• Continuous Quality Improvement
  Emne: QA, QC & GMP, GMP, General conditions, Education, QA, Management tools
  Udbyder: ECA
  Sted: Prague, Czech Republic
  Dato: 16-17 February 2012
  
• Monitoring Clinical Drug Studies: Beginner
  Emne: QA, QC & GMP, Production, Environmental monitoring
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 20-22 February 2012
  
• Preparation, Packaging and Labeling of Clinical Trial Materials
  Emne: QA, QC & GMP, Packaging material, GMP, QC
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 20-21 February 2012
  
• Medical Device Approval Process
  Emne: QA, QC & GMP, Devices
  Udbyder: Barnett International
  Sted: San Diego, CA, USA
  Dato: 27--28 February 2012
  
• Critical Process Cleaning and Cleaning Validation
  Emne: QA, QC & GMP, Validation, Process validation, Cleaning, Cleaning, Validation, US regulation, ICH, EU regulation, Procedures
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 27-29 February 2012
  
• Practical Pharmacovigilance Auditing
  Emne: QA, QC & GMP, Audit-inspection, QA, PQG, Practice
  Udbyder: BARQA
  Sted: Cambridge, England
  Dato: 28-29 March 2012
  
• Good Clinical Practice Auditing - Principles and Practice
  Emne: QA, QC & GMP, Audit-inspection, GCP, Practice, Clinical trials
  Udbyder: BARQA
  Sted: Cambridge, England
  Dato: 28-29 February 2012
  
• Good Clinical Practice for the Laboratory Scientist
  Emne: QA, QC & GMP, QA, GCP, Laboratories, GLP, GMP
  Udbyder: Barnett International
  Sted: San Diego, CA, USA
  Dato: 1 March 2012
  
• GMP Compliance and Auditing for Sterile Pharmaceuticals
  Emne: QA, QC & GMP, GMP, International regulation, Sterile products, Microbiological Quality, GMP, Sterile products
  Udbyder: Key2Compliance
  Sted:
  Dato: Spring 2012
  
• GMP Compliance for Quality Control
  Emne: QA, QC & GMP, QC, GMP, Laboratories, GMP, QC-laboratorium
  Udbyder: Key2Compliance
  Sted:
  Dato: Spring 2012
  
• Pharmaceutical Quality Assurance and Control
  Emne: QA, QC & GMP, QC, Practice, QA, Administration, General principles
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 19-20 March 2012
  
• Drug Quality Fundamentals
  Emne: QA, QC & GMP, Supply/distribution chain, QP, QC, PAT, QA, Process analysis, PAT, Quality by design, CMC, General principles, Pharmaceutical quality, QA, QC
  Udbyder: ACS
  Sted: San Diego, CA, USA
  Dato: 24 March 2012
  
• Introduction to GLP Regulations and Bioanalytical Method Validation by LC/MS/MS
  Emne: QA, QC & GMP, Laboratories, GLP, Analytical methods
  Udbyder: ACS
  Sted: 1) San Diego, CA, USA 2) Philadelphia, PA, USA
  Dato: 1) 27 March 2) May 2012
  
• Auditing for GMP Compliance
  Emne: QA, QC & GMP, Audit-inspection, GMP, GMP, Regulatory compliance
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 27-29 March 2012
  
• Auditing for GMP Compliance
  Emne: QA, QC & GMP, Audit-inspection, GMP, GMP, Inspection, Regulatory compliance
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 27-29 March 2012
  
• Auditing a fictitious API Facility
  Emne: QA, QC & GMP, Audit-inspection, GMP, Practice
  Udbyder: ECA
  Sted: Prague, Czech Republic
  Dato: 27-29 March 2012
  
• Bioassays and Bioanalytics
  Emne: QA, QC & GMP, GMP, Biotech, Biotech, GMP
  Udbyder: ECA
  Sted: Copenhagen, Denmark
  Dato: 27-28 March 2012
  
• Best Practices for Global Investigational Medicinal Product (IMP) Management
  Emne: QA, QC & GMP, Trial supply, Coordinated distribution, GMP, IMP, Pharmaceutical quality, GXP, Supply/distribution chain, Management
  Udbyder: Key2Compliance
  Sted: Copenhagen, Denmark
  Dato: 27-28 March 2012
  
• Statistical Concepts for Non-Statisticians
  Emne: QA, QC & GMP, Statistics, Data analysis, Tools / methods
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 16-17 April 2012
  
• Root Cause Investigation for CAPA
  Emne: QA, QC & GMP, Risk / failure investigations, CAPA, Deviations, RCA
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 17-18 April 2012
  
• Manufacture of highly potent APIs
  Emne: QA, QC & GMP, Production, Risk management, Raw materials, API
  Udbyder: ECA
  Sted: Barcelona, Spain
  Dato: 17-18 April 2012
  
• GMP meets GLP - a practical approach
  Emne: QA, QC & GMP, GMP, Laboratories, General conditions, Laboratories, GMP, GLP
  Udbyder: ECA
  Sted: Internet
  Dato: 23 April 2012
  
• Complying with QS Regulation Requirement
  Emne: QA, QC & GMP, Change control, US regulation, QA, US regulation, QSR
  Udbyder: Barnett International
  Sted: San Fransisco
  Dato: 30 April 2012
  
• Global GCP Monitoring
  Emne: QA, QC & GMP, Audit-inspection, GCP
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 3-4 May 2012
  
• FDA Meetings 101
  Emne: QA, QC & GMP, Pharmaceutical quality, FDA regulation
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 10 May 2012
  
• European Computer Validation Conference – the new Annex 11
  Emne: QA, QC & GMP, Validation, EU regulation, Computer systems, Compliance, Validation, GxP compliance, EU regulation, GMP, Validation, EU regulation, Computer systems
  Udbyder: ECA
  Sted: Copenhagen, Denmark
  Dato: 15-16 May 2012
  
• Drug Product Stability and Shelf-Life
  Emne: QA, QC & GMP, Biotech, Practice, Stability testing, Shelf-Life
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 30 May - 1 June 2012
  
• Advanced GCP
  Emne: QA, QC & GMP, QA, GCP, Audit-inspection, GCP
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 4-5 June 20112
  
• Data Management in the Electronic Data Capture Arena
  Emne: QA, QC & GMP, Document management, CFR, GDM
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 5-6 June 2012
  
• Surviving an FDA Inspection -- FDA Inspections of Non-U.S. Sites
  Emne: QA, QC & GMP, Audit-inspection, Authority inspection, US regulation
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 5-6 June 2012
  
• Documentation Management and Control
  Emne: QA, QC & GMP, Document management, GDP, GMP, Practice
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 7-8 June 2012
  
• Strategies for Setting up and Implementing Supplier Audits
  Emne: QA, QC & GMP, Audit-inspection, Strategy, Supply/distribution chain, Management
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 11-12 June 2012
  
• Pharmaceutical Technology Transfer
  Emne: QA, QC & GMP, QA, Technology Transfer
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 13-14 June 2012
  
• Introduction to Clinical Data Management
  Emne: QA, QC & GMP, QA, Clinical trials, GCP
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 14-15 June 2012
  
• CGMPs In-Depth Analysis for Pharmaceutical Life Cycle Management
  Emne: QA, QC & GMP, GMP, Regulatory compliance, Risk analysis, General conditions, Education
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 18-20 June 2012
  
• Distillation: Design, Operation, and Control
  Emne: QA, QC & GMP, Production, QA, Specific formulations
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 18-20 June 2012
  
• Gap Analysis
  Emne: QA, QC & GMP, Practice
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 22 June 2012
  
• European GMPs and the Role of the QP
  Emne: QA, QC & GMP, GMP, EU regulation, QA, QP
  Udbyder: ECA
  Sted: Bethesda, MD, USA
  Dato: 27-28 June 2012
  
• Procesanalytisk Teknologi
  Emne: QA, QC & GMP, QA, PAT, QC, PAT, Process control, Statistics, Sampling, Analytical chemistry, IR, NIR, Practice
  Udbyder: DTU
  Sted: Lyngby, Denmark
  Dato: May / June 2013
  
• CEO's Business Strategy Design & Implementation Handbook
  Emne: QA, QC & GMP, QA, Management tools
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• FDA Good Laboratory Practices (GLP) Course
  Emne: QA, QC & GMP, Laboratories, US regulation, GLP
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• Pharmaceuticals FDA-cGMP Training (21CFR210-211)
  Emne: QA, QC & GMP, GMP, International regulation, General conditions
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• Six Sigma Training Course
  Emne: QA, QC & GMP, Risk / failure investigations, Six sigma
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• Current Good Manufacturing Practice: An Introduction
  Emne: QA, QC & GMP, GMP, International regulation, General conditions, Inspection
  Udbyder: PERI
  Sted: Internet
  Dato: Ongoing
  
• FDA-cGMP Training (Quality System Requirements -21CFR820)
  Emne: QA, QC & GMP, GMP, International regulation, Devices, US regulation, GMP
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• FDA GMP Training: Online Human Food FDA cGMP Training
  Emne: QA, QC & GMP, GMP, Food, International regulation
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• Effective Investigation and Corrective Actions (CAPA)
  Emne: QA, QC & GMP, Risk / failure investigations, Practice, CAPA, GMP, US regulation
  Udbyder: Globepharm
  Sted: Internet
  Dato: Ongoing
  
• Preparing For, and Passing, an FDA Inspection – guaranteed!
  Emne: QA, QC & GMP, Audit-inspection, Authority inspection, US regulation, GMP
  Udbyder: Globepharm
  Sted: Internet
  Dato: Ongoing
  
• Effective Quality Assurance Auditing
  Emne: QA, QC & GMP, Audit-inspection, Quality audit, US regulation, GMP, ISO, EU regulation, Practice, Psychology
  Udbyder: Globepharm
  Sted: Internet
  Dato: Ongoing
  
• Managing the QC Laboratory in a GMP Compliant Manner
  Emne: QA, QC & GMP, Laboratories, QC-laboratorium, GMP, Inspection
  Udbyder: Globepharm
  Sted: Internet
  Dato: Ongoing
  
• Fundamentals and Essentials of Validation
  Emne: QA, QC & GMP, Validation, IQ / OQ / PQ, International regulation, GMP, Practice
  Udbyder: Globepharm
  Sted: Internet
  Dato: Ongoing
  
• Vandbehandling - DET RENESTE VAND
  Emne: QA, QC & GMP, Water systems, Validation, User requirements
  Udbyder: Holm & Halby
  Sted: Brøndby and Århus, Denmark
  Dato:
  
• ISO 13485:2003 / ISO 19011 Auditor Training
  Emne: QA, QC & GMP, Audit-inspection, ISO, Practice
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• ISO 13485:2003 Training
  Emne: QA, QC & GMP, Devices, ISO
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• ISO 14001:2004 and Environmental Training
  Emne: QA, QC & GMP, QA
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• ISO 14001:2004 Auditor Training
  Emne: QA, QC & GMP, Audit-inspection, ISO, Practice
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• ISO 19011:2002 QMS & EMS Auditor Training
  Emne: QA, QC & GMP, Audit-inspection, ISO, Practice
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• ISO 9000:2000 / ISO 19011 & Auditor Training
  Emne: QA, QC & GMP, Audit-inspection, ISO, Practice
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• ISO 9000:2000 / ISO 19011 Auditor Training
  Emne: QA, QC & GMP, Practice, ISO, Audit-inspection
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• ISO 9000:2000 Overview for Top Management
  Emne: QA, QC & GMP, QA
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• ISO 9000:2000 Training
  Emne: QA, QC & GMP, QA
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• ISO / TS 16949:2002 Training
  Emne: QA, QC & GMP, QA
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• ISO / TS 16949 / ISO 19011 Auditor Training
  Emne: QA, QC & GMP, Audit-inspection, ISO, Practice
  Udbyder: CALISO
  Sted: Internet
  Dato: Ongoing
  
• Good Laboratory Practices (GLPs)
  Emne: QA, QC & GMP, Laboratories, GLP, Regulatory compliance, US regulation
  Udbyder: RAPS
  Sted: Online
  Dato: Ongoing
  
• An Introduction to Good Manufacturing Practice (GMP) for Drug Products
  Emne: QA, QC & GMP, GMP, General conditions
  Udbyder: Zenosis
  Sted: Internet
  Dato: Ongoing
  
• CT09: Preparing for GCP audits and inspections
  Emne: QA, QC & GMP, Audit-inspection, GCP, US regulation, EU regulation, QA
  Udbyder: Zenosis
  Sted: Internet
  Dato: Ongoing