Expertise

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  • Expertise in genomics and transcriptomics

    Expertise in genomics and transcriptomics

    Data Analysis - Analytics August 24, 2015 Check with publisher

    I lead the Integrative Genomics of Ageing Group (http://pcwww.liv.ac.uk/~aging/), and I have extensive experience in data analysis and integration of multidimensional data. Although my lab’s research integrates different strategies, its focal point i...

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  • The Complete Payroll Law and Best Payroll Service 2017

    The Complete Payroll Law and Best Payroll Service 2017

    Pharmacology - Drug Development Baltimore, MD ( Baltimore, MD) February 24, 2017 Check with publisher

    Overview: This course covers a very broad range of topics from worker classification, to employee classification, to establishing methods and rates of pay, what must be included in the rate of pay, hours that must be compensated as worked time, requi...

  • Project Management Business Administration

    Project Management Business Administration

    Engineering Fremont (California) February 21, 2017 Check with publisher

    Overview: This course begins with general principles of Project Management Business Administration (PMBA) and continues to elaborate on specific topics relevant to pre-bid scenarios, execution phase strategies, and close out dilemmas. Why should you ...

  • Statistical Analysis of Measurement Uncertainty : Metrology

    Statistical Analysis of Measurement Uncertainty : Metrology

    Business and Management Fremont (California) February 21, 2017 Check with publisher

    Overview: The webinar begins with an examination of the fundamental vocabulary and concepts related to metrology. Topics include: accuracy, precision, calibration, and "uncertainty ratios". The webinar ends with an explanation of how to combine all r...

  • Effective FDA and ISO Management Reviews

    Effective FDA and ISO Management Reviews

    Pharmacology - Drug Development Fremont (California) February 21, 2017 Check with publisher

    Overview: In this presentation will cover the requirement for management review from FDA cGMP and ISO 13485 and approaches that can make these effective. Management review should be a key part of keeping your quality management system efficient and e...

  • How to Conduct a Human Factors - Test following ISO 62366

    How to Conduct a Human Factors - Test following ISO 62366

    Pharmacology - Drug Development Fremont (California) February 21, 2017 Check with publisher

    Overview: This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for a compliant human factors/ usability validation. HF/U validation is very different from device validation. For example, success criteria is qualitat...

  • Design Inputs Design Outputs Traceability Matrix

    Design Inputs Design Outputs Traceability Matrix

    Engineering Fremont (California) February 21, 2017 Check with publisher

    Overview: If your design and manufacturing resources are spending too much time on documentation and not enough time on actual design and manufacturing you as a manager need to be looking for ways to simplify their work. Areas Covered in the Session:...

  • 1099-MISC:Block By Block Discussion

    1099-MISC:Block By Block Discussion

    Business and Management Fremont (California) February 21, 2017 Check with publisher

    Overview: This course will cover not only these common mistakes but make suggestions regarding the contents of each Block on the Form 1099-MISC. Why should you Attend: Form 1099-MISC is one of the most common Information Reporting Form that businesse...

  • Client Expectations Without Losing Your Shirt or the Next Job

    Client Expectations Without Losing Your Shirt or the Next Job

    Engineering Fremont (California) February 21, 2017 Check with publisher

    Overview: By learning to present issues in the right framework we decrease adversarial behaviors on the project and increase the likelihood that our proposals for additional work will be accepted. Why should you Attend: Our attitudes are the most imp...

  • Acceptance Sampling by Variable inspections

    Acceptance Sampling by Variable inspections

    Business and Management Fremont (California) February 21, 2017 Check with publisher

    Overview: This presentation covers the methods in Z1.9 and shows how to use most common choice, standard deviation unknown. The presentation explains how a simple statistical calculator easily provides the needed sampling statistics. Why should you A...

  • Biologics Facility Design & Pharmaceutical Regulatory Aspects

    Biologics Facility Design & Pharmaceutical Regulatory Aspects

    Pharmacology - Drug Development Fremont (California) February 21, 2017 Check with publisher

    Overview: This course explores some of the best practices of pharmaceutical facility design with an emphasis on regulatory aspects. FDA and other global regulatory body requirements are discussed and the reasoning behind them. Why should you Attend: ...

  • Singapore Seminar on  FDA Data Integrity for Computerized Systems

    Singapore Seminar on FDA Data Integrity for Computerized Systems

    Pharmacology - Drug Development Singapore (Singapore) February 16, 2017 Check with publisher

    Overview: The Problem: We have all heard of Data Integrity but do you really understand what it is? Do you understand how 21 CFR 11 and Annex 11 fit into this picture? Specifically, can you answer questions on the following? • Evolution of 21 CFR Par...

  • Seminar on  21 CFR Part 11 compliance for software validation and SaaS/Cloud

    Seminar on 21 CFR Part 11 compliance for software validation and SaaS/Cloud

    Pharmacology - Drug Development Sao Paulo (Sao Paulo) February 16, 2017 Check with publisher

    Overview: • This interactive two-day course explores proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. • Many companies are outsourcing IT resources and getting invol...