Версия для слабовидящих
Адрес197376, Санкт-Петербург,
ул. Профессора Попова, д. 14, лит. А |
ДеканатФармацевтического факультета:
Факультета промышленной технологии лекарств:
АбитуриентамПриемная комиссия:
8 (812) 499-39-20 (с 20 июня)
|
- Поступающему
- Студенту
- Ранжированный список заявлений на общежитие
- Стипендиальная поддержка
- Перевод с коммерции на бюджет
- Перевод на фармацевтический факультет
- Перевод на факультет промышленной технологии лекарств
- Военно-Патриотический Клуб
- ЭИОС СПХФУ
- Библиотека
- МНО (Молодежное научное общество)
- Студенческий совет
- Профком
- Центр карьеры
- Гранты, олимпиады
- Памятка по профилактики Covid-19
- Мониторинг наркоситуации
- Сотруднику
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- Профилактика экстремизма и терроризма
- Признаки экстремистской организации, признаки вербовки в экстремистскую организацию, последствия участия в экстремистской организации, совершения экстремистских преступлений (правонарушений)
- Информационная безопасность: государственная политика РФ
- Клиническая фармакология наркотических анальгетиков.Вред, причиняемый наркотическими веществами
- Лекция о вреде курения
- Антикоррупция
- Выборы ректора
Оценка составов препаратов «Квинсента» и «Велгия»
В связи с рядом публикаций в СМИ и социальных сетях относительно результатов оценки составов препаратов «Квинсента» и «Велгия», Санкт-Петербургский государственный химико-фармацевтический университет официально заявляет, целью указанного исследования была научно-исследовательская работа по физико-химической экспертизе вышеуказанных ЛС по отдельным показателям без оценочного суждения, по договору с адвокатским бюро.
Таким образом, в рамках проведенного испытания нельзя делать вывод о качестве исследуемых ЛС, так как методики анализа и нормы качества вышеуказанных ЛС, установленные производителем при регистрации, являются собственностью производителя и не были предоставлены в распоряжение исследовательской лаборатории.
Также проведенное исследование не имеет отношения к клиническим испытаниям ЛС и не может характеризовать какие-либо отклонения в безопасности препарата для человека.
Для формулирования выводов о качестве необходимо проведение испытаний вышеуказанных серий ЛС в рамках аттестата аккредитации лаборатории по нормативной документации производителя данных препаратов.
По данным Федеральной службы по надзору в сфере здравоохранения, ее лабораториями перед вводом в гражданский оборот была проведена экспертиза качества по всем показателям 3 серий лекарственного препарата Велгия в 2024 году и 10 серий лекарственного препарата Квинсента (последний - в июне 2025 года). В результате было подтверждено соответствие препаратов установленным требованиям при регистрации.
Отметим, что контроль качества лекарств проводится только в аккредитованных лабораториях при сопоставлении с нормативной документацией производителя, в которой обозначены все параметры состава и качества лекарственного препарата. Лаборатории Росздравнадзора работают в соответствии с данным принципом, контролируя качество и безопасность препаратов.
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