traceable calibrations, FDA regulations, FDA regulation training, FDA pharmaceutical regulation, 21 CFR Part 820, calibration standards, ISO calibration, FDA cGMP regulations, FDA compliance, FDA cGMP, paperless records, 21 CFR Part 11, calibration procedures, calibration traceability, quality calibration program, a paperless calibration department that meets biotech, pharmaceutical, and medical device reqirements, paperless calibration compliance for national and international standards and regulations, virtual calibration workshops

 


Unravel the mystery of paperless calibration compliance for ISO standards & FDA regulations
This new 1 day virtual workshop has been designed to assist the attendee

in developing, managing, improving and/or evaluating a paperless

Quality Calibration Program (QCP) that meets calibration requirements for

21 CFR Part 820.72 (FDA's QSR), 21 CFR Part 58,

21 CFR Part 110, 21 CFR Part 211, 21 CFR Part 606,

and ISO 9001:2008 / ISO 13485:2003 standards. This workshop fulfills the

training requirements mandated by ISO standards and FDA regulations;

and is worth .8 RUs towards any ASQ certification.
(Click here for more detailed information on course objectives)

Workshops can also be given
for your company in-house.
Call or email for details.
If you have questions or need more information,
please send an email to: yokota-69@charter.net
or call: (608) 846-6968