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  • Data Integrity in Clinical Trials in [Latest methods]

    Data Integrity in Clinical Trials in [Latest methods]

    Other Services Fremont (California) September 12, 2018 290.00 Dollar US$

    Overview: The clinical data recording process, however, as inspected/audited by inspectors/auditors is initiated with the recorded data, either in the Case Report Form, or in some other system, or in an electronic database. Why should you Attend: Thi...

  • Mastering Excel [Pivot Tables] in Advanced Technology

    Mastering Excel [Pivot Tables] in Advanced Technology

    Other Services Fremont (California) September 12, 2018 190.00 Dollar US$

    Overview: You can quickly create a compact summary report (based on tons of data) without needing to write complex formulas or rely on lengthy techniques. Why should you Attend: The PivotTable feature is perhaps Excel's best analytical tool and in ad...

  • 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...

  • 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...

  • 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...

  • Analysis Of Extremely Non-normal Data Web Conference by Compliance4all

    Analysis Of Extremely Non-normal Data Web Conference by Compliance4all

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

    Overview: Reliability Plotting is a graphical technique that is a standard method described in some reliability textbooks. The method is used primarily for data that is problematic in one or more of the following ways: non-normal. Why should you Atte...

  • Understanding Autism Spectrum Disorder Web Conference by Compliance4all

    Understanding Autism Spectrum Disorder Web Conference by Compliance4all

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

    Overview: This is an interactive overview of how DMAIC can be utilized in a home environment to improve the quality of life for a child diagnosed as being on the Autism Spectrum. Why should you Attend: Why One in every 68 children is now diagnosed wi...

  • The New FDA-Product Approval Web Conference by Compliance4all

    The New FDA-Product Approval Web Conference by Compliance4all

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

    Overview: The US Food and Drug Administration has recently released information about its new strategies as a result of the new administration. The new commissioner recently announced a new policy for Warning Letters and FDA-483 responses, putting ma...

  • Compliance with FDA and ISO Requirements Web Conference by Compliance4all

    Compliance with FDA and ISO Requirements Web Conference by Compliance4all

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

    Overview: To satisfy QSR and ISO 13485 requirements, medical device companies must respond to field reports swiftly and compliantly. There are certain circumstances in which a report from the field requires the device manufacturer to take steps regar...

  • The Investigational Medicinal Product Dossier Web Conference by Compliance4all

    The Investigational Medicinal Product Dossier Web Conference by Compliance4all

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

    Overview: This 90 minute training course will provide your company the opportunity for comprehensive understanding of the IMPD (Investigational Medicinal Product Dossier) and the structure and content differences between a EU CTA Application and an F...

  • Sampling Plans for Risk Management in Incoming QC Web Conference by Compliance4all

    Sampling Plans for Risk Management in Incoming QC Web Conference by Compliance4all

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

    Overview: The pros and cons of the 2 most widely used sampling plans (ANSI Z1.4, and Squeglia's C=0) are examined in detail, focusing especially on the weaknesses of such plans in regards to meeting regulatory requirements. Real-world examples are pr...

  • FDA Regulation of Combination Products Web Conference by Compliance4all

    FDA Regulation of Combination Products Web Conference by Compliance4all

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

    Overview: A combination product is a product composed of any combination of a drug and a device; a biological product and a device; a drug and a biological product; or a drug, device, and a biological product. Why Should you Attend: To gain a fundame...