Good Clinical Practices (GCP) - Understanding and Implementing the Current Global Requirements

This GCP training course is designed to provide participants with an in-depth understanding of the clinical research process, the roles and responsibilities of key players, as well as, regulatory requirements.

Why Should You Attend:

Upon completion of this course, each participant will have a thorough understanding of the latest updated GCP requirements dictated by FDA, European regulators and ICH requirements for sponsors, monitors, and investigators.

Who Will Benefit:

This GCP training webinar is specifically designed for clinical operations staff as well as GCP auditors and others involved in conducting clinical studies of new medications who require a working knowledge of the regulatory requirements (US and EU) and ICH regulations for Good Clinical Practices (GCPs).

Clinical research managers who oversee and instruct CRMs and CRAs will gain insight into how to best train these employees and how this information can help provide more consistent compliance of the GCP requirements. Other research professionals will also benefit from this GCP training program.

Instructor Profile:

Upon earning a degree in Zoology at North Carolina State University, Joy McElroy made her debut in the pharmaceutical industry in 1992 at Pharmacia & UpJohn performing environmental monitoring and sterility testing. Her hard work allowed her to move into a supervisory role at Abbott Laboratories where she oversaw their quality control lab.

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.

For Registration:

http://www.complianceonline.com/good-clinical-practices-gcp-understanding-and-implementing-the-current-global-requirements-webinar-training-704282-prdw?channel=sciencedz