Since 1st of January 2017, an e-CTD became an obligatory format and method of submission and e-CTD software became indispensable tool for each MAH in the EU. Also, many non-EU health and regulatory authorities follow this path closely [e.g. Health Canada]. Therefore we have decided to expand our range of services.
Daily Archives: 14/06/2017
NEWS
- PharmaVigil Automates PV Literature Activities with PubHive
- We offer services of local PV responsible person for Portugal
- We translate to Ukranian and Russian!
- Our working hours or the quality of our services did not change due to the COVID-19 pandemics
- Tools for e-submission
- Mobile application for reporting adverse drug reactions for medicinal products
- Serialization knocking at the door – what to expect?
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Contact Glad to help you!