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| eLearning
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DIA eLearning is web-based courseware that users can access at any time, from any Internet-enabled location. eLearning program content is developed under the watchful eye of DIA subject matter experts, actively practicing in their professional disciplines, so users receive the same expert content that is presented at traditional DIA meetings and training courses. Most eLearning courses offer continuing education credits. eLearning is available to anyone; DIA membership is not required. | |
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Benefits of DIA eLearning
9 Things You Should Know About DIA eLearning
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DIA eLearning enables DIA customers worldwide to access our expert content and continuing education credits from their home or office. The following eLearning programs are now available: |
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 Clinical Investigator eLearning Program |
DIA's Clinical Investigator eLearning Program provides a unique opportunity for clinical research professionals to learn the regulations, process, and best practices of conducting safe and effective clinical trials. The eLearning program is made up of two modules:
- Study Preparation and Initiation
- Conducting the Study
The eLearning program is an interactive case study that follows a fictitious clinical investigator and his study team through an entire clinical trial. At specific points throughout the story, you make decisions about what actions the characters should take. In this way, you can learn the concepts in context and in a way that greatly promotes learning and retention.
04721 Clinical Investigator: Module 1 - Study Preparation and Initiation
04722 Clinical Investigator: Module 2 - Conducting The Study
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| History of US Drug Regulation eLearning Module |
DIA is offering the History of US Drug Regulation eLearning module free of charge to our customers. We believe this is a topic that would benefit anyone in the pharmaceutical industry or in government, and that this module serves as a great introduction to our eLearning offerings. AND you can receive continuing education credit for the module for a nominal fee.
Click the link below to view the module details in the panel to the right. To access the course, click the link in the Description tab. To request CE credit and take the exam, download the request form using the link in the Continuing Education tab.
05701 History of US Drug Regulation
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| Informed Consent |
This innovative eLearning module uses a detailed case study and examples taken from actual consent forms to provide an in-depth analysis of the key concepts of the informed consent process. Topics covered include the identification of situations that require consent, the proper methods of gaining consent, and the writing of consent forms and related documents for studies with different characteristics. The module also addresses unique situations that do not require consent, alternative methods of communicating consent information to different populations, and changes to informed consent under HIPAA.
05702 Informed Consent
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| Medical Communications eLearning Certificate Program |
Developed exclusively for DIA members by DIA members, each a recognized expert in a given subject, the DIA Medical Communications Certificate Program incorporates industry best practices into a systematic, comprehensive curriculum of nine modules addressing the key aspects of medical communications.
02701 Crisis Management
02702 Database Management
02703 Literature Evaluation
02704 Literature Searching
02705 Medical Inquires
02706 Medical Writing
02707 Product Labeling
02708 Regulatory Issues
06701 Statistics for Medical Communications Professionals
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| Navigating HIPAA eLearning Program |
DIA's Navigating HIPAA eLearning Program reviews the Health Insurance Portability and Accountability Act of 1996 in four interactive modules. The four modules include:
- Overview and Administrative Simplification
- Privacy
- Security
- Electronic Transactions, Code Sets, and Unique Identifiers
The modules examine the rules and regulations set forth by HIPAA legislation, delving into the effects HIPAA has and will have on the industry, and the changes that will need to be made to keep HIPAA-covered entities compliant with the new laws. The modules have been updated to incorporate the latest updates to the regulations, as well as more information on the impact of HIPAA on clinical research. The modules provide an organized framework for approaching HIPAA legislation, plus a list of pertinent government and industry resources.
03721 Navigating HIPAA: Module 1 - Overview and Administrative Simplification
03722 Navigating HIPAA: Module 2 - Privacy
03723 Navigating HIPAA: Module 3 - Security
03724 Navigating HIPAA: Module 4 - Electronic Transactions, Code Sets, and Unique Identifiers
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| Structured Product Labeling |
These modules are designed to provide an informative overview of the key concepts of SPL (structured product labeling). The first module, Practical Overview of SPL and XML, provides information on what SPL is and why it is important to FDA and pharmaceutical companies, as well as provides an overview of the SPL regulatory process.
The second module, History, Business Case, and Solutions, will provide an overview of guidances and regulations for electronic submissions from 1999-2006, as well as describe the history of labeling submissions to FDA, and the SPL solutions and implementation options.
06702 SPL 1: Practical Overview of SPL and XML
06703 SPL 2: History, Business Case, and Solutions
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Continue My eLearning Courses |
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