Conducting Clinical Trials Under ICH GCP
September 28-29, 2016
Philadelphia, PA
CRA & CRC: Beginner Program
September 27-29, 2016
San Francisco, CA
Auditing Techniques for Clinical Research Professionals
October 11-12, 2016
San Francisco, CA

Worldwide Orphan Drug Designation Applications and Requirements

Please check back later for this seminar's current schedule, or review our other live seminars for similar courses.

Course Description

Globally, there is a need for orphan drug research, development, and approval for underserved patient populations who have diseases that affect very few individuals. While this patient population has been largely ignored, some pharmaceutical companies have built their research pipeline around these patients. Receiving orphan drug designation and approval confers many benefits to the developer to compensate for the development costs of the drug. This web seminar will explore which countries allow orphan drug designations, the application requirements, population limits and how to support this number, how the applications are the same, who to submit the application to, if and when the application can be changed, and how it needs to be supported over the development process.

Learning Objectives

  • Identify the countries that have orphan drug designations
  • Identify, on a global basis, the differences and similarities of these applications (and how to re-use the information), including differences in population requirements
  • Discuss the importance of the indication chosen for designation, and how this ultimately affects the final label and how this can differ among countries
  • Examine the most difficult sections of the applications and mitigate agency concerns
  • Discuss the benefits of orphan designation
  • Describe how orphan drug indications and applications can be modified
  • Describe the timing of the application in the drug development process

Who Should Attend

  • Individuals who want an introduction to the orphan drug designation on a global scale
  • Regulatory Affairs Professionals
  • Clinical Research Professionals
  • Research and Development Professionals
  • Project Managers


Cheryl Vitow  

Click here for complete trainer biographies 

Registration Fees


Includes up to 20 participants at one site. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional sites, please call 1-800-856-2556 for pricing.

Accreditation Information

Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 1.5 hours (0.15 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation.  Barnett International will mail ACPE statements within three weeks of program completion.  ACPE#: 0778-0000-11-067-L01-P. Released: 8/11. 

Hold this course at your company! For more information, contact Naila Ganatra at (215) 413-2471.