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  • Funding news shared by Trialect:
    http://r.sib.trialect.com/zpf77tcu8sp3f.

  • Funding news shared by Trialect:
    http://r.sib.trialect.com/zpf77tcu8sp3f.

  • Suzzane Dmello posted an update 3 hours, 2 minutes ago

    Scheduled On : Friday, May 20, 2016 at 13:00 Hrs

    Description :
    This Webinar will focus on the importance of managing FDA oversight of computer system validation in the medical device industry by anticipating and preparing for trends. The type and extent of oversight varies with changes to the economic, political, and business…[Read more]

  • Suzzane Dmello posted an update 3 hours, 3 minutes ago

    Scheduled On : Wednesday, May 18, 2016 at 13:00 Hrs

    If your organization is struggling with understanding the salient requirements associated with the control of documents and records, this webinar is for you. This webinar will help your organization better understand the FDA’s expectations for the control of documents and records, while p…[Read more]

  • Suzzane Dmello posted an update 3 hours, 3 minutes ago

    Scheduled On : Wednesday, May 18, 2016 at 13:00 Hrs

    If your organization is struggling with understanding the salient requirements associated with the control of documents and records, this webinar is for you. This webinar will help your organization better understand the FDA’s expectations for the control of documents and records, while p…[Read more]

  • Suzzane Dmello posted an update 3 hours, 4 minutes ago

    Scheduled On : Friday, May 13, 2016 at 13:00 Hrs

    Any company that has international assignments need to understand the proper way to do payroll for those associates. International Payroll can be very complex between understanding tax treaties to what it hypothetical tax. Plus understanding the different options in international…[Read more]

  • Suzzane Dmello posted an update 3 hours, 4 minutes ago

    Scheduled On : Friday, May 13, 2016 at 13:00 Hrs

    Any company that has international assignments need to understand the proper way to do payroll for those associates. International Payroll can be very complex between understanding tax treaties to what it hypothetical tax. Plus understanding the different options in international…[Read more]

  • Suzzane Dmello posted an update 3 hours, 4 minutes ago

    Scheduled On : Thursday, May 12, 2016 at 13:00 Hrs

    Description :
    HIPAA requires that you are aware of your risk for non-compliance. This webinar will discuss what it takes for you /your organization to complete an internal audit to determine your risk for non-compliance and to identify policies that need to be added.
    Without an audit…[Read more]

  • Suzzane Dmello posted an update 3 hours, 6 minutes ago

    Scheduled On : Wednesday, May 11, 2016 at 13:00 Hrs

    Description :
    For the life science industry, interaction with various regulatory agencies is a must. Successful interactions lead to first time approvals for licensure as well as minimum to no observations during inspections. Successful interactions lead to successful outcomes.
    This…[Read more]

  • Suzzane Dmello posted an update 3 hours, 6 minutes ago

    Scheduled On : Wednesday, May 11, 2016 at 13:00 Hrs

    Description :
    For the life science industry, interaction with various regulatory agencies is a must. Successful interactions lead to first time approvals for licensure as well as minimum to no observations during inspections. Successful interactions lead to successful outcomes.
    This…[Read more]

  • Suzzane Dmello posted an update 3 hours, 7 minutes ago

    Scheduled On : Tuesday, May 10, 2016 at 13:00 Hrs

    Description :
    Various firms are subject to various relevant and applicable federal regulations including, but not limited to, Good Laboratory Practice (GLP), Current Good Manufacturing Practice (cGMP), and Good Clinical Practice (GCP).
    It is important for the industry to accurately…[Read more]

  • Suzzane Dmello posted an update 3 hours, 7 minutes ago

    Scheduled On : Tuesday, May 10, 2016 at 13:00 Hrs

    Description :
    Various firms are subject to various relevant and applicable federal regulations including, but not limited to, Good Laboratory Practice (GLP), Current Good Manufacturing Practice (cGMP), and Good Clinical Practice (GCP).
    It is important for the industry to accurately…[Read more]

  • Suzzane Dmello posted an update 3 hours, 8 minutes ago

    Scheduled On : Tuesday, May 10, 2016 at 13:00 Hrs

    This webinar covers critical issues that any FDA regulated firm should understand to survive regulatory scrutiny. Awareness of the topics, at a minimum, will help you ensure your compliance profile import/export practices and, where appropriate, the need to improve it. Critical issues…[Read more]

  • Suzzane Dmello posted an update 3 hours, 8 minutes ago

    Scheduled On : Tuesday, May 10, 2016 at 13:00 Hrs

    This webinar covers critical issues that any FDA regulated firm should understand to survive regulatory scrutiny. Awareness of the topics, at a minimum, will help you ensure your compliance profile import/export practices and, where appropriate, the need to improve it. Critical issues…[Read more]

  • Suzzane Dmello posted an update 3 hours, 10 minutes ago

    Scheduled On : Monday, May 9, 2016 at 13:00 Hrs

    This webinar will cover easy ways that companies can identify and halt brain drain. Also how companies can use their training and development programs as a way to invest in your employees, show commitment to your employees and create loyalty and engagement – without creating complicated, e…[Read more]

  • Suzzane Dmello posted an update 3 hours, 11 minutes ago

    Scheduled On : Friday, May 6, 2016 at 13:00 Hrs

    Description :
    When designing and developing medical devices it is essential to properly classify your device early on in the process to prevent costly and cumbersome regulatory issues and added or unnecessary work later in the design and development process. The determination process,…[Read more]

  • Suzzane Dmello posted an update 3 hours, 12 minutes ago

    Scheduled On : Thursday, May 5, 2016 at 13:00 Hrs

    Description :
    This seminar will help you understand in detail the application of FDA’s 21 CFR Part 11 guidance on electronic records/electronic signatures (ER/ES) for computer systems subject to FDA regulations. This is critical in order to develop the appropriate validation s…[Read more]

  • Suzzane Dmello posted an update 3 hours, 24 minutes ago

    Scheduled On : Tuesday, May 3, 2016 at 13:00 Hrs

    Description :
    This HR compliance training will be looking at specific considerations regarding the four major HR systems such as compensation, performance management, applicant tracking systems and onboarding systems. It will help you in purchasing and effectively implementing HR technologies…[Read more]

  • Suzzane Dmello posted an update 3 hours, 25 minutes ago

    Scheduled On : Wednesday, May 4, 2016 at 13:00 Hrs

    The inspector will consider the potential risks as identified and documented by the regulated user to assess the fitness for purpose of the particular system(s)”. Risk based compliance is great because when implemented right it helps to reduce overall validation and compliance costs by…[Read more]

  • Clayton Storm Wallington-Beddoe posted an update in the hub Healthcare Research & Content Solutions 5 hours, 32 minutes ago

    ICMR, Sun Pharma join hands to work on new drug development initiatives:-

    The Indian Council of Medical Research is teaming up with pharmaceutical firm Sun Pharma for developing drugs and other effective treatment strategies that will counter diseases that affect India, at the same proportion as Malaria. While both the companies did not…[Read more]

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