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Global Considerations for Regulatory Strategy Development

May 5 2014 8:30AM - May 6 2014 4:00PM | DIA 800 Enterprise Rd Ste 200 Horsham, PA 19044

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Overview 

Most regulatory professionals focus their careers on the regulations of a single country or region such as the US or EU. In order for a global regulatory leader to be truly effective, it is critical to understand the key regulatory issues in all major markets and to apply this knowledge to a global regulatory strategy. Communication between health authorities is increasing, making it vitally important that regulatory leaders develop their strategies with a global view. In addition, current trends in the pharmaceutical industry indicate that more and more companies are expanding their global presence to benefit from the explosive growth being projected in the emerging markets. It is essential, therefore, that a global regulatory leader possess the knowledge and skills necessary to enable successful product registrations in multiple markets around the world.
   
This course will allow participants to understand key requirements for the development and execution of a global regulatory strategy by identifying the strategic and tactical aspects of pharmaceutical development in the US, EU and emerging markets.  Course participants will have the opportunity to apply learning objectives in a hands-on workshop.

Course Level: Intermediate


The DIA training course offerings which are available to pharmaceutical professionals are truly excellent. There is a nice array of topics to choose from and no matter what space you reside in (regulatory, clinical, data management, etc.), you should be able to find something that suits your needs.

What You Will Learn 

  • Survey of the Global Regulatory Landscape
  • Unique Challenges in Emerging Markets
  • Assembling and Working with Global Development Teams
  • Constructing and Implementing Global Regulatory Strategies

Who Should Attend 

Pharmaceutical Professionals with an interest in global regulatory requirements in the areas of:

  • Regulatory Affairs with basic knowledge of investigational and marketing applications
  • Business Development
  • Commercial or Marketing
  • Clinical Development
  • Regulatory CM&C
  • Academic Research

Learning Objectives 

At the conclusion of this course, participants should be able to:

  • Explain the importance of the regulatory strategy in pharmaceutical  development and commercialization
  • Apply key requirements for development in a global market to product strategy
  • Plan for the implementation of the Global Regulatory Strategy across multiple regions
  • Identify development areas requiring special considerations across various regions

Special Offers 

Group Discounts Available! Register 3 and Get the 4th FREE!

Hotel & Travel 

Training Course Location
DIA 
800 Enterprise Road, Suite 101
Horsham, PA 19044

Training Course Location
DIA Worldwide Headquarters
800 Enterprise Road, Suite 101
Horsham, PA 19044

Hotel Information
Staybridge Suites Philadelphia- Montgomeryville
119 Garden Golf Blvd    
North Wales ,  PA   19454
Phone +1-215-393-8899
Fax +1-215-393-8898

A limited number of rooms are available at the reduced rate shown below (DIA is guaranteed until April 18, 2014 or until room block is filled). Attendees should make airline and room reservations as soon as possible.
When making reservations, mention the DIA training course.

Standard Room Rate  $109
Click here for more hotel information

Contact Information 

Registration Questions
Toll Free 1.888.257.6457
Phone +1.215.6100
Fax +1.215.442.6199
Monday-Friday 8:30AM-8:00PM ET
CustomerService@diahome.org

Agenda and Event Logistics
Susan Berkelbach, Event Planner
Phone +1.215.442.6183
Fax +1.215.442.6199
Susan.Berkelbach@diahome.org

Faculty 

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Continuing Education 

Drug Information Association has been accredited as an Authorized Provider by the International Association for Continuing Education and Training (IACET), 1760 Old Meadow Road, Suite 500, McLean, VA 22102; +1.703.506.3275.

As an IACET Authorized Provider, Drug Information Association offers CEUs for its programs that qualify under the ANSI/IACET Standard. Drug Information Association is authorized by IACET to offer 1.3 CEUs for this program. Participants must attend the entire program in order to be able to receive an IACET statement of credit. No partial credit will be awarded.

CERTIFICATE PROGRAMS

These programs are part of DIA’s Certificate Program and are awarded the following:
• Regulatory Affairs Certificate Program: 8 Elective Units each

For more information go to www.diahome.org/certificateprograms

Name Credit Type Max Credits CEU
Global Considerations for Regulatory Strategy Deve IACET 12.50 1.300

Disclosure Policy:

It is DIA policy that anyone in a position to control the content of a continuing education activity must disclose to the program audience (1) any real or apparent conflict(s) of interest related to the content of their presentation and/or the educational activity, and (2) discussions of unlabeled or unapproved uses of drugs or medical devices. Disclosure statements will be included in the course materials.

Statement of Credit:

If you would like to receive a statement of credit, you must attend the course, sign-in at the DIA registration desk each day of the course, and complete the on-line credit request process through My Transcript. To access My Transcript, please go to www.diahome.org, select “Login to My DIA” and you will be prompted for your user ID and password. Select “My Transcript” (left side bar) and “Credit Request” to process your credit request. Participants will be able to download a statement of credit upon successful submission of the credit request. My Transcript will be available for credit requests on two weeks after the last day of the course.

To view DIA’s Grievance Policy, please visit the CE page on the DIA website at www.diahome.org/CE

Registration Fees 

Member

Charitable Nonprofit/Academia Member
$810.00
Member Government
$810.00
Member Standard
$1475.00

Non-Member

NonMember Government
$1035.00
Charitable Nonprofit/Academia Nonmember
$1035.00
NonMember Standard
$1700.00
Group Discounts

Printable Registration Form

Register 3 individuals from the same company and receive complimentary registration for a 4th! All 4 individuals must register and prepay at the same time – no exceptions. DIA will apply the value of the lowest applicable fee to this complimentary registration; it does NOT include fees for optional events or DIA membership. You may substitute group participants of the same membership status at any time; however, administrative fees may be incurred. Group registration is not available online and does not apply to the already discounted fees for government or charitable nonprofit/academia.

To take advantage of this offer, please make a copy of this registration form for EACH of the four registrants from your company. Include the names of all four group registrants on each of the forms and return them together to DIA.

Register Online

Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.

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