Your probability of success increases the earlier and more thoroughly you prepare – our proven processes fully prepare your organization for any regulatory challenges.
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.
Press Releases
Due to the COVID-19 pandemic, the Association of Food and Drug Officials (AFDO) Annual Conference, originally scheduled for June 2020 in Phoenix, AZ, has been canceled. BioTeknica is actively helping AFDO plan for medical device webinars to be held later this year. For the latest information on the webinars and new annual conference date, [...]
BioTeknica and its sister companies, Qualified Data Systems and Synergis, are here for you. We are open and operating at full capacity with the ability to access client technology systems remotely, when necessary. Learn about key elements of our continuity plan… Please be assured that in the event of further [...]
Julie Larsen Receives the Association of Food and Drug Officials (AFDO) Associate Member Award International Honor for Exemplary Success and Leadership in Drug & Medical Device Safety Please be assured that in the event of further disruptions, we are prepared to continue with our services remotely in a secure environment [...]
BioTeknica at Upcoming Conferences: 2015 – 2016 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 [...]
