Results 51 to 60 of about 2,223 (166)

14 MeV neutrons for 99Mo/99mTc production: Experiments, simulations and perspectives [PDF]

, 2018
Background: the gamma-emitting radionuclide Technetium-99m (99mTc) is still the workhorse of Single Photon Emission Computed Tomography (SPECT) as it is used worldwide for the diagnosis of a variety of phatological conditions.99mTc is obtained from99Mo ...
Angelone, Maurizio, Boschi, Alessandra, Capogni, Marco, Capone, Mauro, Cherubini, Nadia, De Felice, Pierino, Dodaro, Alessandro, Duatti, Adriano, Fazio, Aldo, Loreti, Stefano, Martini, Petra, Pagano, Guglielmo, Pasquali, Micol, Pietropaolo, Antonino, Pillon, Mario, Pizzuto, Aldo, Quintieri, Lina, Uccelli, Licia   +17 more
core   +1 more source

Comparison of the State Pharmacopoeia, XIII edition and the European Pharmacopoeia requirements for human plasma products

Регуляторные исследования и экспертиза лекарственных средств, 2018
Russian requirements for main products derived from human plasma used to be laid out in several nonintegrated monographs that have been recently included into the State Pharmacopoeia of the Russian Federation, XIII edition.
A. V. Karyakin, E. D. Skotselyas
doaj  

AN OVERVIEW ON PHARMACOPOEIAS IN THE WORLD AND MONOGRAPH ELABORATION TECHNIQUES [PDF]

, 2020
Pharmacopoeias are official sources that contain national and international rules that must be complied with legally and scientifically regarding substances, materials, drugs, devices and methods used in pharmaceutical field and pharmaceutical production.
YAPAR, Evren ALGIN, ÖZDEMİRHAN, Mehmet Emre   +1 more
core   +2 more sources

Analysis of Current Approaches to Monitoring the Content of Depressor Substances

Регуляторные исследования и экспертиза лекарственных средств
INTRODUCTION. Raw materials of biological origin can contaminate medicines with depressor substances, such as histamine, acetylcholine, bradykinin, serotonin, and prostaglandins.
E. O. Chechetova, T. A. Batuashvili, N. P. Neugodova   +2 more
doaj   +1 more source

Preparation of regulatory documents for sodium heparin [PDF]

, 2020
Heparin is a direct-acting anticoagulant that regulates many biochemical and physiological processes. The quality of each drug or substance entering the market to the consumer, its packaging, storage conditions and shelf life, as well as quality control ...
Aseeva, Natalya Valerevna, Dorozhko, Elena Vladimirovna, Vishenkova, Dariya Aleksandrovna   +2 more
core  

IMPROVING THE SYSTEM OF REGISTRATION OF MEDICINES IN RUSSIAN FEDERATION

Разработка и регистрация лекарственных средств, 2019
This article is devoted to the history of the system of registration of medicines in Russian Federation. The article describes the main stages of formation of the legislative basis of regulation of circulation of medicines in the Russian Federation ...
A. G. Tsyndymeyev, R. I. Yagudina, G. T. Abdrashitova, P. A. Krupnov   +3 more
doaj  

Role of Scientific Centre for Expert Evaluation of Medicinal Products in Setting Current Pharmacopoeial Requirements

Регуляторные исследования и экспертиза лекарственных средств
The State Pharmacopoeia is  a  strategic  document  that  stipulates  safety  and quality standards in Russia. Its current progress directly correlates with the functioning of Scientific Centre for Expert Evaluation of Medicinal Products (Ministry of ...
V. L. Bagirova
doaj   +1 more source

SELECTION OF FLAVOUR ADDITIVES AND METHOD OF THEIR INTRODUCTION IN THE COMPOSITION OF COMPRESSED MEDICATED CHEWING GUMS [PDF]

, 2020
An important characteristic of oral medicines, which include medicated chewing gums, is their pleasant taste. This can be achieved by adding taste coregents to their composition.
Kutsenko, Sergiy, Maslii, Yuliia, Ruban, Оlena   +2 more
core   +2 more sources

Comparative Analysis of Compendial Quality Requirements for Carvedilol Products

Регуляторные исследования и экспертиза лекарственных средств
INTRODUCTION. Carvedilol is a drug used to treat renovascular hypertension and cardiovascular diseases. A monograph for carvedilol drug substance has been included in the State Pharmacopeia of the Russian Federation (SP RF); however, quality requirements
A. I. Belanova, E. V. Lankina, A. A. Taranova   +2 more
doaj   +1 more source

Comparative Analysis of Russian and Foreign Pharmacopoeial Requirements for the Quality Control of Water for Injection: Challenges and Ways of Harmonisation

Биопрепараты: Профилактика, диагностика, лечение, 2019
Parenteral dosage forms are dissolved using sterile water for injection whose quality is regulated by special requirements. The lack of a monograph on sterile water for injection in the State Pharmacopoeia of the Russian Federation, as well as the ...
S. M. Sukhanova, N. M. Minaeva
doaj   +1 more source