Your probability of success increases the earlier and more thoroughly you prepare – our proven processes fully prepare your organization for any regulatory challenges.
ABOUT US
We’re a consulting firm specializing in regulatory compliance, FDA inspection readiness, quality engineering, and validation projects for the medical device, biological, and pharmaceutical industries.
BioTeknica will be participating at the following upcoming conferences. We look forward to seeing you there!
10th Annual FDA news Inspection Summit: November 4-6, 2015 in Bethesda, MD.
The number one event for Quality, Compliance and Inspection Readiness Professionals. Hear from seasoned industry professionals and real-life FDA Investigators on how to respond and handle encounters during your next FDA inspection. Learn data analysis techniques that will improve performance and avoid the Warning Letter via CAPA. Julie Larsen will participate as Co-Chairperson.
13th Annual FDAnews Medical Device Quality Congress: Spring 2016 in Bethesda, MD
Great conference for device and diagnostics professionals interested in the latest quality and compliance topics.
120th Annual Association of Food and Drug Officials (AFDO): June 25-29, 2016 in Pittsburgh, PA
AFDO, an international, non-profit organization, brings together high-level regulatory officials, industry representatives, trade associations, and consumer organizations, to streamline, simplify and clarify regulations. Julie Larsen serves on the AFDO’s Drug, Device and Cosmetic committee and will also be an expert panelist at the conference.
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