Data Management

Listings
  • IT Systems Validation for FDA Regulated Industries

    IT Systems Validation for FDA Regulated Industries

    Data Management san Jose (california) January 31, 2021 Check with publisher

    Based on GxP/GMP requirements, FDA requires that all computer systems that handle data regulated by FDA be validated in accordance with their guidance on computer systems. This is critical to develop the appropriate validation strategy and achieve th...

  • EpiXcan Based Analysis

    EpiXcan Based Analysis

    Data Management (United States ) January 29, 2021 Check with publisher

    MedAI uses EpiXcan, which uses a Bayesian hierarchical model, to improve the accuracy of genes that predicted from tanscriptome-wide association studies data. With the help of Bayesian genetic models, EpiXcan has more power to detect significant gene...

  • BSLMM Prediction

    BSLMM Prediction

    Data Management (United States ) January 29, 2021 Check with publisher

    MedAI uses Bayesian Sparse Linear Mixed Model phenotypic prediction model method to help you improve the prediction accuracy of genome-wide genetic locus information. In addition, we also provide phenotypic prediction services with other prediction m...

  • PrediXcan Based Analysis

    PrediXcan Based Analysis

    Data Management (United States ) January 29, 2021 Check with publisher

    The premise of PrediXcan is that the expression level of genes in the organism is mainly regulated by genetic factors, disease states and some other factors. The purpose of PrediXcan is to establish the relationship between genetically regulated gene...

  • Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers

    Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers

    Data Management san Jose (california) December 18, 2020 1699.00 Dollar US$

    This course will educate you about various key elements of sterility assurance and contamination control such as Cleanroom Regulations, Classification, Sources and types of particles, Design Requirements, Validation/Qualification, Operations, Environ...

  • 21 CFR Part 11 and QMS Software Risk-Based Implementation

    21 CFR Part 11 and QMS Software Risk-Based Implementation

    Data Management san Jose (california) October 29, 2020 Check with publisher

    CGMP-compliant companies must develop / implement formal software controls and usage, starting with proper verification and validation methods. This is an important consideration for a company’s Quality Management System (QMS) and must consider appli...

  • Native Saccharomyces cerevisiae Glyoxalase I

    Native Saccharomyces cerevisiae Glyoxalase I

    Data Management New York (New York) August 13, 2020 1.00 Dollar US$

    Glyoxalase I is universally expressed and involved in the protection against cellular damage due to cytotoxic metabolites such as advanced glycation end products (AGEs). It is an integral component of the detoxification system, catalyzing the convers...

  • Foxy-5

    Foxy-5

    Data Management Shirley (New York) July 20, 2020 Check with publisher

    A Wnt5a peptide mimetic. It has been undergoing clinical trials for the treatment of prostate cancer, colorectal cancer, metastatic colon cancer, metastatic breast cancer, and metastatic prostate cancer. https://www.bocsci.com/foxy-5-cas-881188-51-8-...

  • Using Analytics to Plan Quality (and other Management System) Internal Audits

    Using Analytics to Plan Quality (and other Management System) Internal Audits

    Data Management Fremont, CA (Fremont/CA) November 13, 2019 110.00 Dollar US$

    Overview Preliminary risk assessment (e.g., Likelihood X Impact) and the results of previous audits (e.g., number of NCs) are often used to help prioritize the audit schedule. While these are worthwhile to consider, they do not necessarily reflect th...

  • A straightforward method for meeting FDA Requirements for Design Inputs and Outputs

    A straightforward method for meeting FDA Requirements for Design Inputs and Outputs

    Data Management Fremont (Fremont/CA) September 25, 2019 110.00 Dollar US$

    Overview A robust DIOM can serve as the foundation for meeting FDA requirements and is a useful tool to ensure future iterations, changes, and re-visits to the initial design are clearly documented. A DIOM ensures design information is clearly presen...

  • AML High-Risk Transactions - Identify, Manage, Resolve

    AML High-Risk Transactions - Identify, Manage, Resolve

    Data Management Fremont (Fremont/CA) September 25, 2019 110.00 Dollar US$

    Overview This webinar will discuss the techniques for controlling and managing High Risk Transaction. The Instructor will discuss the parameters for identifying and qualifying transactions as high risk and process and communication to be followed. He...

  • Resolving Conflict and Effective Mediation

    Resolving Conflict and Effective Mediation

    Data Management Fremont (California) August 7, 2019 110.00 Dollar US$

    Overview If you avoid arguments, lie to keep the peace, or believe that hiding behind your desk is better that disagreeing than this webinar is for you. Conflict is not a bad thing, in fact it can a truly positive tool in your professional toolkit if...