Introduction to OPDP/APLB for Agency & Marketing Professionals: Maximizing Material Development and Review (1/2 Day)
UPCOMING DATES:
- TBD
Course Description
This innovative course is for all new Pharma and Biotech marketing professionals, AND public relations and advertising agency professionals responsible for creating promotional pieces, programs, or campaigns (Advertising or PR). If you want to create impactful, compliant programs and materials AND increase the effectiveness and efficiency of your interactions with marketers and copy approval teams, this program is for you. In addition to covering all of the regulatory basics you need to know, we will address the new, rapidly evolving promotion and broader manufacturer communication environment.
Lucy’s vast experience in industry communication, regulatory, marketing and medical disciplines, as well as her FDA communication leadership experience, makes her uniquely qualified to lead this course and to provide colorful, illustrative stories regarding the “why” and “how” behind the regulatory requirements.
Utilizing the relevant laws, regulations, guidance, and actual FDA enforcement letters, Lucy will provide the reasoning behind the copy review team’s evaluation and interpretation of claims and programs. This course is a must for all agency and marketing professionals who want to improve their knowledge of the regulatory, legal, and medical requirements for increasing pitch effectiveness and creating successful, sustainable promotional materials and programs, both marketing and public relations.
Topics covered include, but are not limited to:
- Current regulatory/legal/compliance environment (including FDA and other government agencies, payers, Congress, etc.) and enforcement action examples.
- FDA regulatory requirements, including, but not limited to: truthful and non-misleading, consistent with labeling, fair balance, comparative claims, disease state communications, public relations and press releases, medical conventions/conferences, launch campaign development, internet, social media, patient to patient interaction, paid media, influencers, patient testimonials, celebrity spokespersons, Direct-to-Consumer promotion, new FDA draft guidance documents and their potential impact.
- Innovative marketing tactics and programs, such as virtual reality, micro-targeted marketing (such as geofencing), considerations when developing a compliant overall marketing strategy, and legal and regulatory concerns and considerations when developing internal marketing strategy documents and presentations.
- Proven ways to most effectively work with your clients and their copy approval teams to maximize efficiencies and convert “no” to “yes.”
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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