QA, QC & GMP
Courses from preferred partners
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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
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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
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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
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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
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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
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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
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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
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Observation and Recording for Auditors
Emne: QA, QC & GMP, Audit-inspection, Psychology, Practice, Strategy
Udbyder: BARQA
Sted: Cambridge, England
Dato: 13-14 February 2012
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Good Manufacturing Practice in Pharmaceutical Laboratories
Emne: QA, QC & GMP, Laboratories, GLP, GMP, GMP, Laboratories
Udbyder: BARQA
Sted: Cambridge, England
Dato: 14 February 2012
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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
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Audit Analysis and Reporting
Emne: QA, QC & GMP, Audit-inspection, Management, Practice
Udbyder: BARQA
Sted: Cambridge, England
Dato: 16-17 February 2012
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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
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Monitoring Clinical Drug Studies: Beginner
Emne: QA, QC & GMP, Production, Environmental monitoring
Udbyder: Barnett International
Sted: Philadelphia, PA, USA
Dato: 20-22 February 2012
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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
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Medical Device Approval Process
Emne: QA, QC & GMP, Devices
Udbyder: Barnett International
Sted: San Diego, CA, USA
Dato: 27--28 February 2012
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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
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Practical Pharmacovigilance Auditing
Emne: QA, QC & GMP, Audit-inspection, QA, PQG, Practice
Udbyder: BARQA
Sted: Cambridge, England
Dato: 28-29 March 2012
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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
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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
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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
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GMP Compliance for Quality Control
Emne: QA, QC & GMP, QC, GMP, Laboratories, GMP, QC-laboratorium
Udbyder: Key2Compliance
Sted:
Dato: Spring 2012
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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
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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
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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
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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
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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
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Auditing a fictitious API Facility
Emne: QA, QC & GMP, Audit-inspection, GMP, Practice
Udbyder: ECA
Sted: Prague, Czech Republic
Dato: 27-29 March 2012
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Bioassays and Bioanalytics
Emne: QA, QC & GMP, GMP, Biotech, Biotech, GMP
Udbyder: ECA
Sted: Copenhagen, Denmark
Dato: 27-28 March 2012
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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
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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
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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
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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
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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
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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
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Global GCP Monitoring
Emne: QA, QC & GMP, Audit-inspection, GCP
Udbyder: Barnett International
Sted: Philadelphia, PA, USA
Dato: 3-4 May 2012
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FDA Meetings 101
Emne: QA, QC & GMP, Pharmaceutical quality, FDA regulation
Udbyder: Barnett International
Sted: Philadelphia, PA, USA
Dato: 10 May 2012
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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
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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
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Advanced GCP
Emne: QA, QC & GMP, QA, GCP, Audit-inspection, GCP
Udbyder: Barnett International
Sted: Boston, MA, USA
Dato: 4-5 June 20112
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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
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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
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Documentation Management and Control
Emne: QA, QC & GMP, Document management, GDP, GMP, Practice
Udbyder: CfPA
Sted: Amsterdam, The Netherlands
Dato: 7-8 June 2012
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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
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Pharmaceutical Technology Transfer
Emne: QA, QC & GMP, QA, Technology Transfer
Udbyder: CfPA
Sted: Amsterdam, The Netherlands
Dato: 13-14 June 2012
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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
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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
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Distillation: Design, Operation, and Control
Emne: QA, QC & GMP, Production, QA, Specific formulations
Udbyder: CfPA
Sted: Amsterdam, The Netherlands
Dato: 18-20 June 2012
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Gap Analysis
Emne: QA, QC & GMP, Practice
Udbyder: Barnett International
Sted: Boston, MA, USA
Dato: 22 June 2012
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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
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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
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CEO's Business Strategy Design & Implementation Handbook
Emne: QA, QC & GMP, QA, Management tools
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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FDA Good Laboratory Practices (GLP) Course
Emne: QA, QC & GMP, Laboratories, US regulation, GLP
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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Pharmaceuticals FDA-cGMP Training (21CFR210-211)
Emne: QA, QC & GMP, GMP, International regulation, General conditions
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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Six Sigma Training Course
Emne: QA, QC & GMP, Risk / failure investigations, Six sigma
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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Current Good Manufacturing Practice: An Introduction
Emne: QA, QC & GMP, GMP, International regulation, General conditions, Inspection
Udbyder: PERI
Sted: Internet
Dato: Ongoing
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FDA-cGMP Training (Quality System Requirements -21CFR820)
Emne: QA, QC & GMP, GMP, International regulation, Devices, US regulation, GMP
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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FDA GMP Training: Online Human Food FDA cGMP Training
Emne: QA, QC & GMP, GMP, Food, International regulation
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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Effective Investigation and Corrective Actions (CAPA)
Emne: QA, QC & GMP, Risk / failure investigations, Practice, CAPA, GMP, US regulation
Udbyder: Globepharm
Sted: Internet
Dato: Ongoing
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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
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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
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Managing the QC Laboratory in a GMP Compliant Manner
Emne: QA, QC & GMP, Laboratories, QC-laboratorium, GMP, Inspection
Udbyder: Globepharm
Sted: Internet
Dato: Ongoing
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Fundamentals and Essentials of Validation
Emne: QA, QC & GMP, Validation, IQ / OQ / PQ, International regulation, GMP, Practice
Udbyder: Globepharm
Sted: Internet
Dato: Ongoing
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Vandbehandling - DET RENESTE VAND
Emne: QA, QC & GMP, Water systems, Validation, User requirements
Udbyder: Holm & Halby
Sted: Brøndby and Århus, Denmark
Dato:
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ISO 13485:2003 / ISO 19011 Auditor Training
Emne: QA, QC & GMP, Audit-inspection, ISO, Practice
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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ISO 13485:2003 Training
Emne: QA, QC & GMP, Devices, ISO
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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ISO 14001:2004 and Environmental Training
Emne: QA, QC & GMP, QA
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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ISO 14001:2004 Auditor Training
Emne: QA, QC & GMP, Audit-inspection, ISO, Practice
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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ISO 19011:2002 QMS & EMS Auditor Training
Emne: QA, QC & GMP, Audit-inspection, ISO, Practice
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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ISO 9000:2000 / ISO 19011 & Auditor Training
Emne: QA, QC & GMP, Audit-inspection, ISO, Practice
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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ISO 9000:2000 / ISO 19011 Auditor Training
Emne: QA, QC & GMP, Practice, ISO, Audit-inspection
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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ISO 9000:2000 Overview for Top Management
Emne: QA, QC & GMP, QA
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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ISO 9000:2000 Training
Emne: QA, QC & GMP, QA
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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ISO / TS 16949:2002 Training
Emne: QA, QC & GMP, QA
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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ISO / TS 16949 / ISO 19011 Auditor Training
Emne: QA, QC & GMP, Audit-inspection, ISO, Practice
Udbyder: CALISO
Sted: Internet
Dato: Ongoing
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Good Laboratory Practices (GLPs)
Emne: QA, QC & GMP, Laboratories, GLP, Regulatory compliance, US regulation
Udbyder: RAPS
Sted: Online
Dato: Ongoing
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An Introduction to Good Manufacturing Practice (GMP) for Drug Products
Emne: QA, QC & GMP, GMP, General conditions
Udbyder: Zenosis
Sted: Internet
Dato: Ongoing
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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