Regulatory aspects of Prescription Drug/
biologics advertising and Promotional labeling
JUNE 7, 2012 | 12474
REGISTRATION FEES
member Standard................................................................................................................................................................ $295
Nonmember Standard....................................................................................................................................................... $385
member government/Charitable Nonprofit/Academia........................................................................................ $150
Nonmember government/Charitable Nonprofit/Academia .............................................................................. $235
group Site............................................................................................................................................................................... $799
this online training course will address the regulatory requirements for
promotion of prescription drugs and biologics and the role of regulatory
affairs in reviewing promotional labeling.
•;Similarities and differences in regulatory requirements for drugs and
biologics
this course is designed for individuals in pharmaceutical, biologics and
medical device companies and organizations involved in:
• marketing
• Legal
• Regulatory
•;Public relations/affairs
•;Explain the regulatory requirements for prescription drug advertising
and promotional labeling, including preapproval promotional
activities
•;Summarize the principles for advertising and promotion
•;List the required elements for advertisements and promotional
labeling
Regulatory considerations for clinical Development
Programs
JUNE 11, 12, 13, 2012 | 12476
REGISTRATION FEES
member Standard................................................................................................................................................................ $695
Nonmember Standard....................................................................................................................................................... $785
member government/Charitable Nonprofit/Academia ....................................................................................... $350
Nonmember government/Charitable Nonprofit/Academia .............................................................................. $435
group Site............................................................................................................................................................................. $1,750
Learn the basic regulatory requirements for clinical trials designed to
support a New Drug Application in the US.
•;those who have attended any of DIA’s previous regulatory affairs
training courses, will benefit from this in-depth training series on the
regulatory requirements for clinical trials
