PIL Readability Testing is Mandatory in EAEU
February 15, 2022
Ukrainian government simplifies registration of medicines from the U.S., EU and certain other developed countries
On June 16, 2016, the President of Ukraine signed the Amendments to the Medicines Act, which are intended to simplify the procedure of state registration of medicines coming from countries with strong established regulatory requirements, institutions, and procedures. The changes will become effective starting from their official publication day and responsible government agencies must still adjust certain bylaws to implement them.
Extended list of medicines subject to the simplified procedure.
Now all medicines (drugs) registered by a competent authority of the USA (i.e., FDA), Switzerland, Canada, Australia, Japan, and the EU are now subject to the simplified registration procedure. Whereas the previous version of the Medicines Act allowed such simplified procedures only for medicines that treat tuberculosis, HIV/AIDS, viral hepatitis, oncological, and rare (orphan) illnesses. Read Full article HERE.


Пользовательское тестирование по ЕАЭС – обязательная процедура
February 14, 2022
One More Inpharmatis Team Member Gets PhD in Pharmaceutical Sciences
January 27, 2022
В штате Inpharmatis стало на одного доктора фармацевтических наук больше
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Pharma 4.0: Data-Driven Regulation
January 18, 2022
Pharma 4.0: от управления на основе документов к решениям, основанным на данных
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New Inpharmatis Russian Office Phone Number
January 05, 2022
Изменение контактных данных российского офиса Inpharmatis
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Inpharmatis Team Participated in the Russian Healthcare Forum
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Inpharmatis принял участие в работе форума «Российская неделя здравоохранения»
December 16, 2021