Course overview
Course details
5天
Duration
Parexel学院认证讲师
Faculty
完成 ICH-GCP 培训
Prerequisites
Aim
参与者
Your benefits
计划概述
接触
Aim
为了始终确保受试者和患者的安全和福祉,临床试验需要按照最高质量标准并按照国家和国际指南进行。
参与者
本次研讨会基于对良好临床实践 (ICH-GCP)、法律框架、伦理考虑以及所有人的角色和责任的充分理解,为参与者提供有效监控临床试验进行所需的必要技能和知识。参与审判的各方。
Your benefits
计划概述
接触
额外的预包装课程
今天开始
我们开发量身定制、有意义且有效的教育和培训计划,以满足生物制药行业对专业人士和高管日益增长的需求。要了解有关我们的计划和定制培训选项的更多信息,或索取免费建议,请联系我们讨论您的需求和期望的目标。
Read our blogs
Just like everything else we do, we put our heart and soul into our blog. Stay in the know with these 3-5 minute quick but informative reads. We genuinely hope our shared insights make your life a little easier.
Empowering Clinical Trial Sites: Parexel Academy’s Commitment to Excellence in Global Research
In the dynamic world of clinical research, clinical trial sites are the crucial nexus where innovation meets patient care, generating vital data that drives scientific
10 月 2, 2024
Interview with a vPGC Graduate
We’re always looking for ways to solicit feedback on our programs to improve them for future learners. Recently, we sat down for a chat with
9 月 9, 2024
ICH-GCP, AI (Artificial Intelligence), and Machine Learning: The Future of Drug Development
Introduction Clinical trials play a critical role in the development of new drugs, but they are often associated with inflated costs, long durations, and low
5 月 2, 2024