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Julia:ReplicateBE – release 0.2.0

Опубликовано 26 октября, 201926 октября, 2019 frozencat

doiGitHub

Вот и подоспел релиз 0.2.0 для оценки параметров смешанной модели репликативного дизайна биоэквивалентности по методу С (EMA) – FDA model.

 

Рубрики: IT, Julia, Mixed Model, Биоэквивалентность

Навигация по записям

Предыдущая запись: ClinicalTrialUtilities: обзор
Следующая запись: Тест ClinicalTrialUtilities и ReplicateBE на Raspberry Pi 4

Свежие записи

  • Long WS Wide: или про то, как выполнить анализ разницы изменений между группами
  • Частые вопросы: Регистрация и экспертиза по правилам ЕАЭС
  • Главные ошибки при формировании базы данных в MS Excel
  • Тест ClinicalTrialUtilities и ReplicateBE на Raspberry Pi 4
  • Julia:ReplicateBE – release 0.2.0

Галерея

IMG-20170807-WA0032
20170730 175153
DJI 0025
DJI 0034
IMG-20170806-WA0047
20180816 164633 029
  • Human medicines European public assessment report (EPAR): Actelsar HCT, telmisartan,hydrochlorothiazide, Date of authorisation: 13/03/2013, Revision: 19, Status: Authorised
    Source: EMA - Human medicines: European public assessment reports (EPARs) Published on 2025-05-13
  • Human medicines European public assessment report (EPAR): Enbrel, etanercept, Date of authorisation: 02/02/2000, Revision: 75, Status: Authorised
    Source: EMA - Human medicines: European public assessment reports (EPARs) Published on 2025-05-13
  • Human medicines European public assessment report (EPAR): Dyrupeg, pegfilgrastim, Date of authorisation: 28/03/2025, Revision: 2, Status: Authorised
    Source: EMA - Human medicines: European public assessment reports (EPARs) Published on 2025-05-13
  • Compounding Quality Center of Excellence | Engage with the Compounding Quality Center of Excellence
    Source: FDA - What's New: Drugs RSS Feed Published on 2025-05-13 By FDA
  • Human medicines European public assessment report (EPAR): Datroway, datopotamab deruxtecan, Date of authorisation: 04/04/2025, Status: Authorised
    Source: EMA - Human medicines: European public assessment reports (EPARs) Published on 2025-05-13
  • IXCHIQ
    Source: FDA - What's New: Vaccines, Blood & Biologics RSS Feed Published on 2025-05-13 By FDA
  • Tissue Guidances
    Source: FDA - What's New: Vaccines, Blood & Biologics RSS Feed Published on 2025-05-12 By FDA
  • Allergenics
    Source: FDA - What's New: Vaccines, Blood & Biologics RSS Feed Published on 2025-05-12 By FDA
  • eSubmitter Application History
    Source: FDA - What's New: Vaccines, Blood & Biologics RSS Feed Published on 2025-05-12 By FDA
  • Development & Approval Process (CBER)
    Source: FDA - What's New: Vaccines, Blood & Biologics RSS Feed Published on 2025-05-12 By FDA
  • Untitled Letters
    Source: FDA - What's New: Drugs RSS Feed Published on 2025-05-12 By FDA
  • FDA and CDC Recommend Pause in Use of Ixchiq (Chikungunya Vaccine, Live) in Individuals 60 Years of Age and Older While Postmarketing Safety Reports are Investigated: FDA Safety Communication
    Source: FDA - What's New: Vaccines, Blood & Biologics RSS Feed Published on 2025-05-12 By FDA
  • Human medicines European public assessment report (EPAR): Xyrem, sodium oxybate, Date of authorisation: 13/10/2005, Revision: 37, Status: Authorised
    Source: EMA - Human medicines: European public assessment reports (EPARs) Published on 2025-05-12
  • GDUFA Type II API DMF Payment Receipts Report
    Source: FDA - What's New: Drugs RSS Feed Published on 2025-05-12 By FDA
  • Human medicines European public assessment report (EPAR): Dimethyl fumarate Mylan, dimethyl fumarate, Date of authorisation: 22/04/2024, Revision: 2, Status: Authorised
    Source: EMA - Human medicines: European public assessment reports (EPARs) Published on 2025-05-12
Предыдущие записи
Тема: Scaffold от Danny Cooper.