CRO Oversight MasterClass
26 & 27 May, 2022
CRO Oversight online masterclass provides an overview of the key concepts and best practices for CRO management in a global clinical trial setting.
This online training provides an overview of the key concepts and best practices for CRO management in a global clinical trial setting. It also includes information about the global regulatory landscape regarding CRO management, primarily focusing on EMA, FDA, and ICH E6(R2).
26 & 27 May, 2022, Virtual
Time Zone: Eastern Standard Time (EST) / UTC−05:00
This is a topic that is important to all Sponsors that are outsourcing clinical trial duties or activities to support the factors that are critical to success of their product development. This CRO online training provides an overview of the key concepts and best practices for Clinical Research Organization (CRO) management in a global clinical trial setting. It also includes information about the global regulatory landscape regarding CRO management, primarily focusing on EMA, FDA, and ICH E6(R2).
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Who should attend?
This course is designed for clinical research personnel who are involved in the selection, oversight, and management of CROs and other vendors. It is ideal for sponsor clinical trial leaders, clinical project managers, and others involved in decision-making regarding vendors.
"High attention to detail in course content and very well delivered"
Product Development Manager
"Very good training led by two knowledgeable and open experts. Excellent insight given on many complex topics. Interactive and highly useful"
USP PD Team Manager
"Great course, impressed with the knowledge of the trainers and ability to answer wide variety of questions!"
Manager, Senior Investigator
MT Sword Laboratories (BMS)
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