
Planning a Health Canada PRCI Compliant Submission Blog Post
How to set yourself up for a successful Health Canada PRCI submission
How to set yourself up for a successful Health Canada PRCI submission
In the last few years, the pharmaceutical industry has invested in developing Complex Biologics including proteins, oligonucleotides, viral vectors, and engineered cells. One area within Complex Biologics experiencing tremendous growth…
多个共性因素可显著影响从最终数据库锁定(DBL)到上市申请提交的周期。Speaking from first-hand experience across more than 50…
儿科 PBPK 模型在药物开发流程中具有广泛应用,正日益广泛用于优化并替代临床研究,However, the approach has yet to become fully…
Do expensive bioequivalence studies stall your generic drug approval? Learn how you can streamline complex generic drug development with our white paper.
The European Medicines Agency (EMA) recently approved dulaglutide (Trulicity®) at higher doses (3 mg and 4 mg solutions). Dulaglutide is indicated for the treatment of adults with insufficiently controlled type…
BY ROMAN CASCIANO, OPINION CONTRIBUTOR — 03/29/21 05:30 PM EDT No one is happy with the price of drugs nor how we pay for them: not patients, not the lawmakers who…
Join us on 2021 年 4 月 21 日, 星期三, from12:00 PM – 2:00 PM EDT for Certara’s first annual Strategic Evidence & Value Communication Symposium. Across two panel discussions, a host of Certara and industry experts will debate and explore various best practices to ensure effective communication of product value, as well as the expanded use of Real World Evidence to accelerate market access decision-making.
众多药企苦于原料药(DS)与制剂(DP)杂质的表征及如何将其整合至监管申报资料。This webinar is designed to increase the…