n this digest you will find the most important news on registration, safety and quality management of medicinal products in Azerbaijan, Armenia, Belarus, Georgia, Kazakhstan, Kyrgyzstan, Moldova, Mongolia, Tajikistan, Turkmenistan, Ukraine and Uzbekistan, which entered into force at the end of 2018 and in the first half of 2019. The most significant news in brief: In Armenia On […]
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Medicines: news on registration, pharmacovigilance and quality management in CIS
Seminar on language requirements in Ukraine
Joint seminar related to the influence of new language policy on the medical market operators has been hosted by Cratia and Association of Medical Device Market Operators (www.amomd.com). On the event we spoke on the influence of Law of Ukraine dd April 25, 2019 “On assurance of functioning of the Ukrainian language as state language” […]
Law on state language of Ukraine
On May 16, 2019, the Law of Ukraine “On Ensuring the Functioning of the Ukrainian Language as the State Language” (hereinafter – “the Law”) was published. The Law will enter into force on July 16, 2019, and transitional periods of 6 months have been set for a significant part of the provisions. The Law has […]
Changes in procedure of state registration of medicines, Ukraine
On April 9, 2019, the Resolution of the Cabinet of Ministers of Ukraine No. 296 came into force and approved amendments to the Resolution of the Cabinet of Ministers of Ukraine No. 376 of May 26, 2005 “On approval of the procedure for state registration (reregistration) of medicines and fees for their state registration (reregistration)” and to the Order […]
News on medical devices in Ukraine, February 2019
1. All medical devices that include radio equipment (Wi-Fi, Bluetooth, GPRS and other radio communication modules) must comply with the Technical Regulations of the radio equipment approved by Decree of Cabinet of Ministers of Ukraine No.355 as of May 24, 2017 and when placing on the market, must be accompanied with relevant Declaration of conformity. […]
Uzbekistan introduces a simplified medicines registration procedure
On October 25, 2018, the Procedure for recognition of results of the other countries registration entered into force, approved by Decree of the Cabinet of Ministers of the Republic of Uzbekistan No. 862 dated October 24, 2018 “About approval of the Regulations on procedure for recognition of results of the registration of medicines conducted outside […]
Introduction of mandatory marking using the units of the International System of Units (SI)
From January 1, 2019, the symbols for use in the labeling of all products put into circulation in the territory of Ukraine, should be indicated in accordance with the Regulations, approved by the Order of the Ministry of Economic Development and Trade No. 914. Specifically, units of measurement should be indicated using those of the […]
Regulatory digest for medical devices in Ukraine
We have issued digest regarding regulatory environment for medical devices in Ukraine: 1. Accreditation and designation of three conformity assessment bodies for medical devices has been cancelled in 2018: SE “SMCC”, SE “Cherkasystandartmetrolohiya”, “Politoks” LLC. We have summarised their stories and suggested specific actions for the manufacturer or it’s Authorised representative to be taken towards […]
Regulatory affairs digest of the first half of 2018 for CIS region
In this digest you can find the most important news on issues of registration, safety management, and quality of medicinal products in post-soviet countries: Azerbaijan, Armenia, Belarus, Georgia, Kazakhstan, Kyrgyzstan, Moldova, Mongolia, Tajikistan, Turkmenistan, Ukraine, and Uzbekistan for the first half of 2018: Open file in PDF The highest activity has been observed in the Eurasian Economic Union (ЕАEU): […]