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AMGEN. OUR MISSION: TO SERVE PATIENTS

Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools…

BEST TECHNICAL DIRECTOR COMPETITION ANNOUNCED

Dear Colleagues,   Technical Director is one of the key figures in ensuring that a pharmaceutical company operates in compliance with the requirements of the Good Manufacturing Practice. To popularize…

MAIN FOCUS OF VI ALL-RUSSIA GMP CONFERENCE 2021 AGENDA

The VI All-Russia GMP Conference with international participation will be held on 22–24 September 2021 in a hybrid format. The offline part will take place in St. Petersburg, in the business space…

SEPTEMBER 17: WORLD PATIENT SAFETY DAY

In 2020, this date is celebrated for the second time. Last year, in 2019, in its 72nd session the World Health Assembly passed resolution WHA72.6 “Global action on patient safety” and…

THE RUSSIAN PHARMACEUTICAL INSPECTORATE HAS PROVEN WORTH

The Vth All-Russia GMP Conference with International Participation will take place on September 30 and October 1. Its agenda addresses the implementation of the rules of Good Manufacturing Practice in the…

NEW DEVELOPMENTS IN THE EAEU REGULATIONS

THE BOARD OF THE EURASIAN ECONOMIC COMMISSION HAS PASSED TWO GUIDELINES THAT REGULATE THE PROCESS OF PHARMACEUTICAL DEVELOPMENT AND VALIDATION OF EQUIVALENT EFFICACY AND SAFETY OF MICELLAR DRUGS AND NANODRUGS.…

LETTER CALENDAR: SATURDAY

IN NOVEMBER 2020, CHANGES ARE THOUGHT TO TAKE EFFECT TO RESOLUTION NO. 1361 OF THE GOVERNMENT OF THE RUSSIAN FEDERATION DATED 5 SEPTEMBER 2020, WHICH DEFINES THE RULES OF INSPECTING…

WHAT IS IN THE PROGRAMME OF V GMP-CONFERENCE?

On the official site of V All-Russia GMP-conference with international participation published a business program of the event. Thanks to the online format, Conference organizers were able to ensure the…

БУКВЕННЫЙ КАЛЕНДАРЬ: СУББОТА

Предположительно в ноябре 2020 года нас ждет вступление в Силу изменений к Постановлению Правительства РФ № 1361 от 5 сентября 2020 года, которое определяет правила проведения инспектирования производителей лекарственных средств…
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