UL PURE™ Learning has partnered with corporate and government clients in the Life Science, Health Care, Energy and General Industry markets for over 30 years.
We currently maintain more than 500 eLearning courses that are written and reviewed by recognized subject matter experts, including the USFDA. In fact, more than 1 million industry professionals, including over 36,000 FDA investigators, have completed over seven million courses since 2003. Courses are regularly updated to reflect the most current expectations and requirements of regulators and industry groups. Our global qualityand compliance management methodology has resulted in measurable performance and compliance improvements.
Our eLearning philosophyis based on Mastery Learning, which has been proven to improve retention and change behavior in adult learners through methods thatinclude interaction with dynamic content and built-in assessments.
Hiring is an important factor in creating a solid workforce, and firing is a tool to ensure productivity. This course provides techniques for making good hiring decisions, terminating employees in a consistent and fair manner, and avoiding lawsuits resulting from the hiring and firing process. Topics in this course include: Regulations, Hiring, Interviewing, Testing, and Firing. After completing this course, learners should recognize several tools that will assist in the hiring and firing processes. Learners will also identify how to handle difficult employee situations.
Because microbiological and particulate contamination can potentially cause serious health problems in animals and humans, it is vital that sterile products be manufactured, filled, and packaged in an aseptic environment. This course will address the general principles and practices necessary to assure product sterility and safety related to aseptic processing. Topics in this course include: Cleanroom Requirements, The Process, Employee Practices, Validation, and Monitoring. After completing this course, learners will be able to recognize the general principles and practices necessary to ensure product sterility and safety, as well as the Good Manufacturing Practices (GMP) requirements for areas where aseptically produced products are handled.
Documentation is an essential part of Good Manufacturing Practice (GMP). This course provides an overview for manufacturers of pharmaceutical and biological products of the documents required and the controls that should be in place. The regulatory requirements of FDA are addressed with reference also made to the requirements of the EU.The course provides an introduction to staff at all levels and highlights the personal responsibility they have for ensuring documentation is followed and documentation is correct.
This course describes your responsibility for protecting any personal information that is under your control. Topics in this course include: Consequences, Personal Information, Laws, EU Regulations, and Reporting Problems. After completing this course, learners will be able to recognize what personal data must be protected according to the law and our company policies, as well as your personal responsibility in protecting this information. Learners will also be able to identify the risks involved in compromising personal data and know the basic guidelines for safeguarding it.
This course will provide definitions and examples of conflicts of interest, as well as provide guidance and reporting mechanisms for conflicts of interest.
This course will provide definitions and examples of conflicts of interest, as well as provide guidance and reporting mechanisms for conflicts of interest.
