Month: 2017年4月
Clinical Study Protocols: How to Write to Solve Problems Now and Avoid Big Ones in the Future
The identification of different responsibilities, under the clear leadership of the medical writer, is necessary to improve the quality of clinical study protocols – to prevent problems and mistakes that can result later, during conduct of the clinical trial, or afterwards, when reporting on trial results.
Modeling & Simulation for Drug Development & Formulation
A look at how to leverage modeling and simulation technology to enhance all phases of the drug development process.
AI技術によるレギュラトリーライティングの革新
Did you know that you’re likely using artificial intelligence (AI) in your everyday life? For example, the digital music service, Spotify, creates “mood-based” playlists that are curated to users’ musical preferences. Spotify generates these customized play lists using a machine learning algorithm that has learned your unique musical preferences based on your previous interactions with … Continued
Certara、薬物動態 (PK) データを
作成・解析・送信するための
総合的なソリューションを導入
PRINCETON, NJ – Apr. 19, 2017 – Certara today announced the launch of a new solution for preparing, analyzing and submitting PK data in Clinical Data Exchange Standards Consortium (CDISC) format. CDISC supports the acquisition, exchange, submission and archiving of non-clinical and clinical data.
仮想空間に語りかける:創薬業界のバーチャル・ワークプレースの課題
In this webinar, Drs. Peter Bonate and Stacey Tannenbaum discussed what kind of technology tools can facilitate a connection with your audience and address the difficulties of speaking into the ether. They offered practical solutions that you can use to strengthen your collaboration in the virtual workplace.
Certara’s d3 Medicine Partners with the Australian Department of Defence
PRINCETON, NJ – Apr. 5. 2017 – Certara today announced that its d3 Medicine company has been selected to conduct a national audit of Australia’s medical countermeasures (MCM) product research and development (R&D) capabilities and capacity.