The Ad/Promo Review Process: Best Practices (1/2 Day)

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UPCOMING DATES:

  • 11/29/22 (10:00AM - 1:00PM EST)

Course Description

This innovative course provides information designed to decrease pain and increases efficiency. Focusing on copy approval best practices, it is a must for all Pharma and Biotech professionals responsible for designing or ensuring efficiency of the copy review process. Considering all disciplines and each process point, this program explores mechanisms to greatly improve the copy review process, resulting in greater process efficiency and improved materials quality. The goal - markedly decrease “vicious cycling” – perhaps to one review cycle!

Lucy’s vast industry experience in medical, regulatory, and marketing disciplines, as well as her extensive work in designing and improving copy review processes for hundreds of companies, makes her uniquely qualified to lead this course and to provide colorful, illustrative stories regarding the “why” and “how” behind the best practices.

If you believe your process could be improved, or are constantly being asked to improve it, this course is for you.

Topics covered include, but are not limited to:

  1. The top 10 copy approval process imperatives.
  2. Reviewer and submitter (champion) roles and responsibilities
  3. Increasing multi-disciplinary team effectiveness
  4. Meeting preparation considerations
  5. Maximizing agency interactions and expectations

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

REGISTER NOW

To register, please fully complete the registration form below, including checking the box agreeing to the terms, then click submit. 






This program and all materials supporting the program are intended for educational purposes only. They are not intended to provide legal, regulatory or risk advice or guidance regarding any specific situation or scenario and are not a substitute for the advice of your advisors on specific issues. This material is based on the laws and regulations  and  DDMAC/OPDP/APLB enforcement letters in place at the time of the presentation and reflects the individual opinions of Lucy Rose and Associates, LLC.  Because regulations change and risk evaluation is a subjective matter, the information  and opinions provided and expressed  as part of the program should not be relied upon for decision-making purposes. Further, Lucy Rose and Associates, LLC does not warrant or guarantee that you or your employer or any of its employees or contractors, by relying on the educational materials provided by the program, would not be subject to regulatory or  legal enforcement actions. This material is copyrighted ; it or any part of it may not be photocopied, reproduced, disseminated ,or otherwise used by anyone other than Lucy Rose and Associates, LLC  without the express written prior authorization of  Lucy Rose and Associates, LLC.

Each individual paid registration is for one attendee. The program may not be shared with anyone other than a paid registrant either during its live presentation or in any recorded format.

The program or any part of it may not be recorded or reproduced in any format including but not limited to: video, photographs, screen shots, audio recordings or by any other mechanism in existence now or in the future capable of reproducing or transmitting the program in whole or in part.

Copyright 2022 by Lucy Rose and Associates, LLC.  All rights reserved.