Pharmaceutical quality management services from j3i Value Added CQA Services Contact j3i on +44 118 977 1736 for international clinical quality management services

eLearning for Clinical Research and the Pharmaceutical Industry

A cost-effective, flexible solution to training staff and partners. Sometimes it's just not practical to provide face-to-face training for every person who could benefit, which is where our eLearning packages excel.

EU Clinical Trial Directive eLearning CD Screenshotj3i's eLearning is truly multimedia: with sound, pictures and video taking learners through their course at their own pace. The courses are Flash based and designed to run in any web browser on any operating system. Completion and competency test and certification options are available as required.

 

The following modules are currently available:

 

European Clinical Trial Directives - covering the Clinical Trial Directive 2001/20/EC, the GCP Directive 2005/28/EC and the GMP Directive 2003/94/EC. This module is suitable for sponsor staff responsible for managing trials within the European Union. Click here to download a product brochure.

GCP Overview - covering objectives, definition and principles of GCP. This module is suitable for sponsor staff or new employees who need to have a general introduction to GCP. Click here to download a product brochure.

GCP for Monitors - covers objectives and definitions of GCP, global legislative frameworks and monitoring activities. This module allows sponsors to ensure that monitors have a detailed understanding of their responsibilities with regard to GCP. Click here to download a product brochure.

GCP for Investigators and Study Site Staff - this module outlines GCP, provides an overview of the various legislative frameworks and details the responsibilities of Investigators with regard to GCP. Using this module, sponsors can ensure that the investigators they choose to carry out studies have a detailed understanding of GCP and their specific responsibilities. Click here to download a product brochure.

UK Clinical Trial Statutory Instruments - covers the various SI's used in the UK to govern clinical trials. This module is directed at sponsor staff who are responsible for managing trials within the UK. Click here to download a product brochure.

UK Clinical Trial Statutory Instruments for Investigators and Study Site Staff - covers the various SI's used in the UK to govern clinical trials. This module is aimed specifically at Investigators and allows a sponsor to ensure that the investigators they choose to carry out studies in the UK have a detailed understanding of their responsibilities required by the SI's. Click here to download a product brochure.

 

Request a Demonstration CD for any of the above modules

Email info@j3iquality.com to request a demonstration CD. Include your name, company, address and telephone number, along with some brief details of who you are thinking of using the package for.

The demonstration CD allows the user to understand how the eLearning package works, see the quality of production and explore the topics covered.

 

If you have a requirement for a course that isn't listed then contact Julie Meeson detailing your requirement and we will consider it for production.

 

Bespoke eLearning Development for the Pharmaceutical Industry

j3i can both customise our existing eLearning packages or create tailored solutions to our clients' requirements. Whether it's re-branding an existing course, an idea for a new public course, or a bespoke in-house eLearning project we would be delighted to hear your thoughts.