The Sunshine Act Reporting for Clinical Trials

This webinar will discuss the disclosure requirements for clinical investigators under the Sunshine Act. It will discuss the details of the processes; provide templates for reporting formats; and timelines for reporting.

Why Should You Attend:

The Sunshine Act exposes the physicians and sponsors to new reporting requirements which are unprecedented in their scope and detail noncompliance to which would lead to hefty fines.

Who Will Benefit:

This webinar will provide valuable information to

Principal and co-investigators participating in industry-sponsored clinical trials

Sponsors of clinical trials

Legal experts involved in assisting physicians and patients alike with medical malpractice

Medical accounting companies

Instructor Profile:

Dr. Mukesh Kumar is a Washington DC-based consultant in regulatory affairs and quality assurance for manufacturers and developers of FDA-regulated products. He leads the regulatory affairs and quality assurance departments at Amarex, a full service pharmaceutical product development company based in Germantown, MD.

Note:

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

For Registration:

http://www.complianceonline.com/the-sunshine-act-reporting-for-clinical-trials-webinar-training-702970-prdw?channel=sciencedz