ppt 12 aug

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Clinical Trial Regulations With ICH GCP E6 R2 Workshop Clinical Trials Event Date 17 – 19 September, Location – Amsterdam, The Netherland MASTERCLASS OVERVIEW ON WORLDWIDE CLINICAL TRIALS

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AURELIUS GLOBAL MASTERCLASS.:

AURELIUS GLOBAL MASTERCLASS .

About Us:

About Us “Aurelius Corporate Solutions wants to be seen and accepted as one stop shop for all industry specific master-classes across the globe, thereby making the line managers well versed with the acceptable technology and business practices, adopted worldwide.”

Clinical Trial Regulations:

Clinical Trial Regulations Complexity and cost of  clinical trials  have increased dramatically in recent years. Learn how evolutions in technology and risk management process offer new opportunities to increase efficiency and focus on relevant activities and  clinical trial protocols . Understand how the new guidelines and regulations allow  clinical trial research  taking strategic decisions that benefit your organization’s success.

WHO SHOULD ATTEND CLINICAL TRIALS TRAINING? :

WHO SHOULD ATTEND CLINICAL TRIALS TRAINING? Clinical Development Manager should attend this clinical trials training. Clinical Operations Manager should attend this clinical trials training. Director Clinical Development should attend this clinical trials training. Director Clinical Operations should attend this clinical trials training. Head Of Clinical Operations should attend this clinical trials training. Head Of Regulatory Affairs should attend this clinical trials training.

Date &venue:

Date &venue 17 – 19 September Ramada Apollo Center Amsterdam, The Neaterland

More Queries?:

More Queries? Email - masterclass.registrations@aurelius.in Phone - +44 2032 398083

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