Biotech and Pharmaceutical Companies:
Meeting the FDA requirements
for traceable calibration;
also included:
Paperless Records -
Designing and Creating Your
Own Electronic Forms.
This new 2.5 day workshop has been designed to assist the attendee
in developing, implementing, improving and/or evaluating a
Quality Calibration Program (QCP) that meets the
Quality System Regulation (QSR - FDA cGMP requirements),
ISO 9000, and ISO 13485 standards. This workshop fulfills the
training requirements mandated by ISO standards and FDA regulations;
and is worth 1.6 RUs towards any ASQ
certification.
(Click here for
more detailed information on course objectives)
The workshop will be held at
Promega Corporation,
Madison, Wisconsin.
Click here for directions.
Attendees receive a handout booklet on
A QCP for Biotech and Pharmaceutical Companies,
a video CD, and a copy of the book -
Paperless Records.
(Lunch is included the first two days)
Discounts available for:
Multiple attendees,
WBMA and NCSLI members
Workshops can also be given
for your company in-house.
Call or email for details.
The workshop will be held at
Promega Corporation,
Madison, Wisconsin.
Click here for directions.
Attendees receive a handout booklet on
A QCP for Biotech and Pharmaceutical Companies,
a video CD, and a copy of the book -
Paperless Records.
(Lunch is included the first two days)
Discounts available for:
Multiple attendees,
WBMA and NCSLI members
Workshops can also be given
for your company in-house.
Call or email for details.
