Regulatory Challenges in the CIS and Russia - TOPRA In CEE WebinarNovember 22, 2023
Thanks 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.
Особенности выбора типа Пользовательского тестирования листка-вкладыша в ЕАЭСNovember 01, 2023
Features of Choosing the Type of PIL RUT in EAEUNovember 01, 2023
PIL Readability User Testing in EAEU Special Autumn OfferOctober 25, 2023
Специальное Осеннее Предложение по пользовательскому тестированию листка-вкладышаOctober 24, 2023
PIL Readability Testing is Mandatory in EAEUFebruary 15, 2022
Пользовательское тестирование по ЕАЭС – обязательная процедураFebruary 14, 2022
One More Inpharmatis Team Member Gets PhD in Pharmaceutical SciencesJanuary 27, 2022
В штате Inpharmatis стало на одного доктора фармацевтических наук большеJanuary 27, 2022
Pharma 4.0: Data-Driven RegulationJanuary 18, 2022