OPDP/APLB Data Expectations: A Deep Dive for Medical Professionals (1/2 Day)
UPCOMING DATES:
- 6/14/23 (10AM-1PM EST)
- 9/20/23 (10AM-1PM EST)
**If new as a medical reviewer, we strongly encourage this course be taken in tandem with the Introduction to OPDP/APLB Review for Medical Professionals on 6/13/23 and 9/19/23**
Course Description
This innovative intermediate course, focusing on data quality and claim support, is a must for all Pharma and Biotech MEDICAL PROFESSIONALS responsible for reviewing promotional pieces, programs, or campaigns in the copy review system. If you want to increase your confidence AND increase the effectiveness and efficiency of your work in the copy approval team, this program is for you. This program is a true deep dive into understanding data requirements for promotional claims AND understanding the role of the medical professional in this context.
Lucy’s vast experience in industry medical, regulatory, and marketing disciplines, as well as her training and previous work as a physician assistant, makes her uniquely qualified to lead this course and to provide colorful, illustrative stories regarding the “why” and “how” behind the regulatory requirements as related to your medical review.
Utilizing the relevant laws, regulations, guidance, and numerous actual FDA enforcement letters, Lucy will provide an understanding of, and the reasoning behind, the regulations regarding data requirements, providing a firm foundation for your contribution. OPDP for Medical Professionals is a must for all medical professionals who want to improve their knowledge of the regulatory, legal, and medical requirements regarding data support and how they apply to the medical review.
Topics covered include, but are not limited to:
- FDA regulatory data requirements for claims, including, but not limited to: comparative claims, patient testimonials, secondary claims, patient preference claims, adherence claims, cost effectiveness claims, patient reported outcomes claims, quotations, press releases, peer-to-peer communications, patient to patient communications, celebrity spokespersons, new FDA draft guidance documents and their potential impact, importance of context, data representation, study interpretation, study design requirements, etc.
- Proven ways to most effectively work with your copy approval teams to maximize effectiveness and your medical knowledge contribution.
Participants may NOT receive a refund for any reason (unless LRA cancels course). If the participant cannot attend the course they may send a substitute. Course registration may be transferred to another participant at any time by notifying lucyrose01@aol.com prior to the start of the course.
Price: $750.00
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To register, please fully complete the registration form below, including checking the box agreeing to the terms, then click submit.