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The PDA/FDA Joint Regulatory Conference is celebrating a milestone!
For 25 years, industry professionals
have been taking advantage of this exclusive forum to hear directly
from FDA experts regarding current Agency efforts and potential
impacts on the development of global regulatory strategies.
When you attend the 2016 PDA/FDA Joint Regulatory Conference,
you will benefit from Center and Compliance updates delivered by the
regulators, hear their perspectives on application reviews, quality, clinically relevant specifications, international efforts, and more. Industry
experts from leading pharmaceutical companies will also present case
studies illustrating how they employ these global strategies in their
daily processes.
This year’s Conference, with the theme Aligning Manufacturing Goals with Patient Needs through Successful Innovation and Compliance,
will feature over twenty sessions highlighting the development of
innovative medical products while balancing patient safety.
In homage to the 25-year PDA-FDA
collaboration, this year’s event will also offer retrospectives on the
last 25 years and the challenges industry may face in the future such as
changes that will need to be implemented to keep up with new
technology.
Register before July 1 and save up to $600!
Immediately following the Conference, from Sept. 14-15, PDA will be hosting the 2016 PDA Data Integrity Workshop, which
will explore quality culture, human behavior, training needs and
technology requirements to help attendees get a broad perspective on
common factors, cause and effect of data integrity issues. Through round
table discussions, attendees will learn about best practices for
preventing, detecting, mitigating and remediating data integrity issues.
Ample opportunity will be provided for networking with industry peers,
regulators and solution providers to enhance the overall learning
experience.
Register now!
And, to round out the week, from Sept. 15-16, to complement what you learned at the Conference, PDA’s Education Department will be hosting six courses on how to establish an effective GMP auditing program, implement quality risk management for pharmaceutical and biotechnology manufacturing operations, prepare for regulatory inspections for the FDA and EMA and the best practices for investigations.
Don’t wait! Register today. |
 Parenteral Drug Association (PDA)
4350 East West Highway, Suite 600 Note new suite number!
Bethesda, MD 20814 USA
Tel: +1 (301) 656-5900
Fax: +1 (301) 986-1093
www.pda.org
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