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news and events
news
Zenosis releases a new version of Module SUB06 on variations to marketing authorisations in Europe
Zenosis announce IT advances that offer yet more to their clients
Zenosis launches 'The DCP: The Decentralised Procedure'
Zenosis launches 'The NDA process: Requirements for obtaining approval for a new drug in the USA'
Zenosis achieves 21 CFR part 11 Validation
Zenosis launches 'The ANDA: Requirements for obtaining approval for a generic product in the USA'
Zenosis launches 'Preparing for a GCP audit or inspection'
Zenosis launches 'The IND: How to gain approval for Clinical Trials in the USA'
Zenosis launches 'Clinical trial monitoring: Study monitoring, documentation and closure'
Zenosis launches 'Clinical trial monitoring: Site evaluation and set-up'
Zenosis announces major systems enhancements
Merry Christmas from Zenosis
Zenosis launches 'Introduction to Clinical Trials in India'
Zenosis launches 'Registration of Monoclonal Antibodies'
Zenosis launches 'Introduction to ICH Good Clinical Practice (ICH-GCP)'
Zenosis launches 'An Introduction to GMP for Drug Products'
Zenosis launches 'Pharmacokinetics and Pharmacodynamics in Drug Registration'
Zenosis launches 'Third Generation' modules
GeneEd and Zenosis announce strategic partnership
Zenosis moves into the Indian Market
Dr Francisco Harrison joins Zenosis Board
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