Regulatory Challenges in the CIS and Russia - TOPRA In CEE Webinar
November 22, 2023Thanks to all who participated in Pharmacovigilance Strategy Course
At the end of April we had an intensive two days of pharmacovigilance training with focus on GVP guidelines. We hope that all participants gained new knowledge and got an insight of how system changes will affect the day-to-day pharmacovigilance operations within the pharmaceutical companies by learning from practical examples, which are based on real life situations.
Thanks to all who participated and especially to our brilliant trainer José Alberto Ayala Ortiz (M.Sc. Pharm. and M.Sc. IT) who has experience both from the Regulatory (Danish Medicines Agency), and from the Pharmaceutical Industry, where he has been responsible for Pharmacovigilance IT systems, databases and Electronic transmissions in Project Manager role.


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PIL Readability User Testing in EAEU Special Autumn Offer
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Специальное Осеннее Предложение по пользовательскому тестированию листка-вкладыша
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PIL Readability Testing is Mandatory in EAEU
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Пользовательское тестирование по ЕАЭС – обязательная процедура
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One More Inpharmatis Team Member Gets PhD in Pharmaceutical Sciences
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В штате Inpharmatis стало на одного доктора фармацевтических наук больше
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Pharma 4.0: Data-Driven Regulation
January 18, 2022