Zenosis provide 'always up-to-date' e-learning and knowledge support for Regulatory and Compliance professionals working within the global Life Science industry.

Following the release of Zenosis' first monitoring title; 'Clinical trial monitoring: Site evaluation and set-up', our latest release 'Clinical trial monitoring: Study monitoring, documentation and closure' compliments this by covering the responsibilities and procedures associated with monitoring processes and close-out visits. These modules are aimed at staff familiar with clinical development. Topics include monitoring of Case Report Forms (CRFs), Source Document Verification (SDV) and essential documents for collection and review.

For information on other modules please view our catalogue, where a 14 day free trial can also be arranged.

If you would like one of our sales team to contact you to explain how so many global pharmaceutical and biotech companies are bringing about a paradigm shift in the effectiveness of their regulatory and compliance training and performance support, please send us a mail with a suggested time and date you would like us to call.