RAPS Florida Chapter: Developing Regulatory Affairs Expertise—Key Practices to Increase Knowledge Base

Come engage with professionals from your local regulatory community for breakfast and an interactive presentation on ways to develop your regulatory expertise. This event is coordinated by the RAPS Florida Chapter and is intended to encourage knowledge sharing and community development. Continental breakfast will be provided, compliments of EMMA International Consulting Group Inc., and RAC holders may claim two RAC recertification credits.

In today’s competitive market, you need regulatory and business insight to provide more value on project teams and achieve smoother agency reviews. But developing quality experience and expertise in regulatory is not solely based on the time spent compiling regulatory applications. We will share several practices and resources that can help you enhance your knowledge base and make you more effective in your role.

This presentation is intended to familiarize regulatory associates, specialists and managers with practical strategies to help them or their department gain expertise. Specifically, the presentation will cover how to better anticipate FDA concerns, provide informed assessments and improve business decision-making. It will cover a range of recommended practices that can be implemented to broaden and deepen your pool of regulatory experience.




  • At a Glance
  • Objectives
  • Agenda
  • Speaker
  • Registration Info
  • Cancellation

At a Glance

Date:

Tuesday, 23 May 2017 (8:00–10:30 am EDT) 

Location:

CONMED
11311 Concept Boulevard
Building 2, QES Room
Largo, FL 33773
+1 727 392 6464

Directions are available online.

RAC Credits:

Two RAC certification credits upon completion of the program. 

Registration Fees:

Prior to 16 May 2017
RAPS Members: $20
List: $30

On or after 16 May 2017
RAPS Members: $30
List: $40

Seating is limited. Advance registration is required; no onsite registration is available. Register early to secure a seat.

Objectives

At the conclusion of this program, you should be able to:

  • Identify different resources to gain key business and product-related information
  • Make use of FDA’s warning letters website, submission databases and past product reviewss
  • Understand how these tools can improve regulatory decision-making

Agenda

Tuesday, 23 May 2017

8:00–8:30 am            Registration Check In, Networking and Breakfastr
8:30–10:00 am           Speaker Presentation
10:00–10:30 am         Interactive Question and Answer Session

Speaker

Penny Daniels, 3D Communications

Registration Info

Prior to 16 May 2017
RAPS Members: $20
List: $30

On or after 16 May 2017
RAPS Members: $30
List: $40

>> Registration Online

>> Registration Form (PDF) – for registration by mail or fax.

Contact RAPS Solutions Center at +1 301 770 2920, ext. 200, or email raps@raps.org to learn about the special student registration rate.

Other Information

RAPS reserves the right to cancel this program at its sole discretion. RAPS will not be responsible for travel or other costs incurred due to cancellation.

Questions? Call RAPS Solutions Center at +1 301 770 2920, ext. 200, or email raps@raps.org.

Program Contact

Local Contact: Jan G. Flegeau, chair, RAPS Florida Chapter

RAPS Contact: Wesley Carr, senior program manager, chapter and volunteer relations

Cancellation

Registration fees for this event are nonrefundable. Substitutions may be accepted with written approval from RAPS. If you have questions or concerns, please contact RAPS customer service at +1 301 770 2920, ext. 200, or via email at raps@raps.org.