Clinical

Listings
  • Molecular Dynamics Simulation

    Molecular Dynamics Simulation

    Clinical Shirley (New York) April 28, 2019 Check with publisher

    Profacgen studies molecular dynamics of protein systems using state-of-the-art software tools. The general workflow of our MD simulation service follows these steps: First, a model system is selected, in which missing segments are fixed and the proto...

  • Regulatory Requirements for Batch Record Review

    Regulatory Requirements for Batch Record Review

    Clinical Fremont (California) October 11, 2018 Free

    Overview: A strong batch record review system is essential in order to properly document all critical processing parameters that go along with the production and manufacture of pharmaceuticals, biologics, medical devices, etc. Areas Covered in the Se...

  • Inactivated RSV Antigen

    Inactivated RSV Antigen

    Clinical Shirley (New York) April 28, 2019 10.00 Dollar US$

    Human respiratory syncytial virus (HRSV) belongs to Paramyxoviridae family. It is a syncytial virus that causes respiratory tract infections. RSV is an enveloped RNA virus with a non-segmented single-stranded negative-sense genome. The disease caused...

  • Recombinant EBV Protein [His]

    Recombinant EBV Protein [His]

    Clinical Shirley (New York) May 30, 2019 10.00 Dollar US$

    The Epstein–Barr virus (EBV), also called human herpesvirus 4 (HHV-4), is named after Michael Anthony Epstein. It is one of the eight known human herpesvirus types in the herpes family, and is common in human diseases. It is best known as the cause o...

  • GMP Environment- Best Practices for Foundational Employee Success

    GMP Environment- Best Practices for Foundational Employee Success

    Clinical Fremont (California) December 12, 2018 150.00 Dollar US$

    Overview: FDA expectations provide some of the framework regarding types and frequency of training, there are decisions that the company will need to make in light of its evaluation of how to best achieve compliance for its employees, maintain a qual...

  • Food Safety - Food Defense 2019

    Food Safety - Food Defense 2019

    Clinical Fremont (California) December 12, 2018 150.00 Dollar US$

    Overview: Food Safety Modernization Act of 2010 was signed into law by President Obama on January 4, 2011, Food Defense is now clearly called out and must be adhered to. Why should you Attend: This webinar will focus on Food Defense and will detail w...

  • Current Trends in CyberSecurity Threats to Medical Devices 2019

    Current Trends in CyberSecurity Threats to Medical Devices 2019

    Clinical Fremont (California) December 12, 2018 150.00 Dollar US$

    Overview: In this webinar, you will learn just how cyberattacks threaten medical devices and how industry is currently responding to them. Why should you Attend: In this webinar, you will learn just how cyberattacks threaten medical devices and how i...

  • Equipment Validation, Tracking, Calibration and Preventive   Maintenance

    Equipment Validation, Tracking, Calibration and Preventive Maintenance

    Clinical Fremont (California) December 12, 2018 150.00 Dollar US$

    Overview: Prior to use, however, this equipment must be validated to make sure it produces product that meets its specifications. There are ways, though, to validate equipment already in use. Areas Covered in the Session: Preventive Maintenance Requi...

  • What is Human Factors and why is it Important?

    What is Human Factors and why is it Important?

    Clinical Fremont (California) January 23, 2019 150.00 Dollar US$

    Overview: This webinar provides a fundamental level appreciation of human factors and how it has been implemented within the engineering discipline to improve design and operation to support system goals. Why should you Attend: Understand the definit...

  • Export Certificate for Medical Devices - Out Your Competition!

    Export Certificate for Medical Devices - Out Your Competition!

    Clinical Fremont (California) January 23, 2019 150.00 Dollar US$

    Overview: The rules that companies must follow when exporting medical devices depend on whether or not their devices have been approved or cleared by the Food and Drug Administration. Why should you Attend: In submitting export certificates, any mist...

  • Understanding and Implementing a Technology Transfer Process

    Understanding and Implementing a Technology Transfer Process

    Clinical Fremont, CA (California) March 20, 2019 150.00 Dollar US$

    Overview The purpose of this training is to provide you with an overview of the Technology Transfer. Define technology transfer. Identify New Product transfer process. Identify elements of the business process framework for managing technology transf...

  • Reprocessing Reusable Medical Devices - Cleaning and Labeling Requirements

    Reprocessing Reusable Medical Devices - Cleaning and Labeling Requirements

    Clinical Fremont, CA (California) March 20, 2019 150.00 Dollar US$

    Overview This training program will explain the rationale, the legal requirements and some methods commonly used for reprocessing and validating reusable medical devices. Why should you Attend Any firm reprocessing another manufacturer's medical devi...