CDER Small Business Regulatory Education for Industry (REdI) Pharmaceutical Quality Symposium July 20-21, 2016

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CDER Small Business and Industry Assistance (SBIA) invites you to join us for this two-day in-depth exploration into the world of pharmaceutical quality. Interact with FDA’s subject matter experts from our Office of Pharmaceutical Quality (OPQ) as we address topics such as:
  • Microbial Controls
  • Manufacturing Process
  • Facilities Assessment
  • Method Validation
…. and many more
This 2 day conference has been pre-approved by RAPS as eligible for up to 12 credits towards a participant’s RAC recertification upon full completion
Keynote Speaker:
Michael Kopcha, Ph.D., R.Ph., Director, Office of Pharmaceutical Quality/CDER/FDA
Registration: This forum will be delivered in hybrid format. When you register you will choose to attend either “In-Person Onsite” or “Virtually Online via Adobe Connect.” You will NOT be able to make changes after you register, so if you are unable to attend, please email us at cancelation@SBIAevents.com
We ask that you please honor your registration commitment to help us plan and deliver this event efficiently.
Accommodation: We have a block of rooms at a discounted rate, that will be available on a first-come, first-served basis until June 22, 2016 onlydisclaimer icon, or until the block is filled. Please reserve your room within our room block now. You will be responsible to pay for your own accommodations. Please be mindful of the hotel’s policies on check-in/checkout and cancellation.

Presentation Information

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(866)-405-5367 | (301)-796-6707 | CDER Small Business and Industry Assistance




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