Services

Listings
  • New European Clinical Trial Regulation Web Conference by Compliance4all

    New European Clinical Trial Regulation Web Conference by Compliance4all

    Other Services Online (California) November 11, 2016 150.00 Dollar US$

    Overview: This course covers the newly proposed requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Regulation 536/2014 (for Drugs, Biologics & Combination Products). The course also covers rec...

  • Corrective and Preventive Action Web Conference by Compliance4all

    Corrective and Preventive Action Web Conference by Compliance4all

    Other Services Online (California) November 11, 2016 150.00 Dollar US$

    Overview: Medical Device managers, engineers, QA personnel, as well as lean program leaders. Do you find yourself constantly struggling to create, manage, and maintain all of the information found in Corrective and Preventive Actions (CAPA)which is o...

  • Spreadsheets in FDA Regulated Environments Web Conference by Compliance4all

    Spreadsheets in FDA Regulated Environments Web Conference by Compliance4all

    Other Services Online (California) November 11, 2016 150.00 Dollar US$

    Overview: Excel® Applications are widely used in laboratories, offices and manufacturing e.g., for data capture, data manipulation and report generation. Regulations such as FDA's GxPs and 21 CFR Part 11 require users of software and computer systems...

  • GMP requirements for quality control and contract laboratories 2017

    GMP requirements for quality control and contract laboratories 2017

    Quality Control, Safety & Security Singapore (Singapore) October 26, 2016 1895.00 Dollar US$

    Overview: Quality control and related contract laboratories are considered at high risk because after testing and approval, drug products and Active Pharmaceutical Ingredients (APIs) are released to the market without further check. That's the reason...

  • GMP requirements for quality control and contract laboratories 2017

    GMP requirements for quality control and contract laboratories 2017

    Quality Control, Safety & Security Singapore (Singapore) October 26, 2016 1895.00 Dollar US$

    Overview: Quality control and related contract laboratories are considered at high risk because after testing and approval, drug products and Active Pharmaceutical Ingredients (APIs) are released to the market without further check. That's the reason...

  • Design Verification data and Process Validation 2016

    Design Verification data and Process Validation 2016

    Quality Control, Safety & Security Houston (Texas) October 26, 2016 Free

    Overview: This 2-day seminar provides a 1-day introduction to the statistical tools used to analyze Design Verification data and Process Validation results. The entire 2nd day is spent on Statistical Process Control and Process Capability Indices. Th...

  • FDA Concepts for Medical Device Companies - Regulations, Myths, Challenges, and Best Practices

    FDA Concepts for Medical Device Companies - Regulations, Myths, Challenges, and Best Practices

    Drug Development Baltimore (MD ) October 26, 2016 Free

    Overview: This seminar will show you how to structure and optimize your QMS. It all starts with Management Responsibility and a commitment to quality. We'll discuss the concepts of management responsibility, a culture of quality, and continuous impro...

  • Statistical Process Control & Process Capability – GlobalCompliancePanel 2016

    Statistical Process Control & Process Capability – GlobalCompliancePanel 2016

    Quality Control, Safety & Security Baltimore (Maryland) October 26, 2016 Free

    Overview: This course teaches participants the fundamental concepts and methods needed to establish effective control charts and estimate process capability. In addition to learning traditional control charts (e.g. xbar, r/s), participants will be ex...

  • Conference on Validation and Part 11 Compliance of Computer Systems and Data 2016

    Conference on Validation and Part 11 Compliance of Computer Systems and Data 2016

    Training and Teaching Zurich (Zurich) October 26, 2016 Free

    Overview: Analytical and other equipment should be qualified and computer systems should be validated to demonstrate suitability for the intended use. Electronic records must comply with FDA Part 11 and EU/PICS GMP Annex 11 requirements to ensure dat...

  • Boston Analytical Pharmaceutical and Medical Device Testing Services

    Boston Analytical Pharmaceutical and Medical Device Testing Services

    Chemical Methods Salem (New Hampshire) October 3, 2016 Check with publisher

    Boston Analytical, the Life Sciences Division of Alpha Analytical, is a cGMP compliant, FDA/DEA registered, ISO/IEC-17025:2005 certified analytical laboratory located in Salem, NH. Boston Analytical provides testing services to the Pharmaceutical and...

  • Boston Analytical Pharmaceutical and Medical Device Testing Services

    Boston Analytical Pharmaceutical and Medical Device Testing Services

    Quality Control, Safety & Security Salem (New Hampshire) October 3, 2016 Check with publisher

    Boston Analytical, the Life Sciences Division of Alpha Analytical, is a cGMP compliant, FDA/DEA registered, ISO/IEC-17025:2005 certified analytical laboratory located in Salem, NH. Boston Analytical provides testing services to the Pharmaceutical and...

  • DOE and SPC for Process Development and Validation 2016

    DOE and SPC for Process Development and Validation 2016

    Quality Control, Safety & Security Philadelphia (Pennsylvania) October 3, 2016 Free

    Overview: This course will present the procedures that must be used in the application of DOE and SPC to the development, design and monitoring of manufacturing and testing processes. A practical approach with case studies and examples will be used, ...