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NEWS

April 17, 2020

The State Expert Center of the Ministry of Health has launched an information resource - covid19.dec.gov.ua on the use of drugs in COVID-19

The State Expert Center of the Ministry of Health of Ukraine has launched an information resource – covid19.dec.gov.ua, which informs about the action of drugs that are currently used in the prevention and treatment of COVID-19.

May 21, 2020

Developed and posted on the website of the Ministry of Health of Ukraine
for public discussion a draft order "On approval of the Procedure for termination
of the registration certificate for a medicinal product and Regulations
on the Commission of the Ministry of Health of Ukraine for termination
of the registration certificate for a medicinal product"

On May 21, the draft order of the Ministry of Health of Ukraine was published on the website of the Ministry of Health of Ukraine for public discussion, proposing to approve the Procedure for Termination of a Drug Registration Certificate and the Regulations on the Commission of the Ministry of Health of Ukraine

May 21, 2020

A draft order "On approval of Amendments to the Procedure
for import of unregistered drugs, standard samples, reagents
into the territory of Ukraine" for public discussion has been developed
and posted on the website of the Ministry of Health of Ukraine

On May 21, the draft order of the Ministry of Health of Ukraine was published on the website of the Ministry of Health of Ukraine for public discussion, proposing to approve the Procedure for importing unregistered drugs, standard samples and reagents into Ukraine.

May 12, 2020

On the recognition of documents issued by the regulatory authorities of the European Economic Area, the United Kingdom concerning the manufacture of medicinal products

The European Commission, the Coordination Group on Mutual Recognition and Decentralized Procedures for Medicinal Products for Human Use (“CMDh”), and the European Medicines Agency (EMA) have jointly developed guidelines on the regulatory requirements for medicinal products for human use. the time of the COVID-19 pandemic.” One of the paragraphs (paragraph 2.2) of the document provides for the extension of valid at the time of announcement (March 12, 2020) by the World Health Organization (WHO) pandemic caused by COVID-19, certificates of compliance with the requirements of good manufacturing practice (certificate GMP) and licenses for the right to conduct business in the manufacture of medicinal products, issued by the regulatory authorities of the European Economic Area (EEA) and the United Kingdom.

EVENTS

February 25, 2020

Sixth scientific-practical conference with international participation "Clinical trials of drugs in Ukraine: new challenges and responses to them“

On October 8-09, 2020, the Sixth Scientific and Practical Conference with International Participation “Clinical Trials of Medicines in Ukraine: New Challenges and Responses to Them” is planned to be held in Kyiv, organized by the State Expert Center of the Ministry of Health of Ukraine.

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Contact information​

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