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What Is It?
Today, validation plays
an ever-increasing role in the pharmaceutical industry
as it is enforced throughout the entire supply chain to
ensure safety, compliance and regulation.
Many companies are still
faced with validation challenges such as
standardization, efficiency, quality, resource
management…etc. Adopting an automated validation
process regardless of whether you are validating a new
piece of equipment, COTS software or a new LIMS system
can result in tremendous cost saving and increased
efficiency.
On May 29th, Compliance
Associates will be holding a FREE seminar at which
delegates will gain knowledge on how to simplify the
validation process as well as expedite the validation
life cycle.
Why Attend?
You will gain insight on
how to expedite your deliverables while enhancing
compliance to accommodate changing industry regulations.
You will also learn how to improve your validation life
cycle by simplifying the validation process to reduce
projects from months to weeks.
Attendees will also get
a sneak preview of Validator 4.0.0 and its automated
functionalities. Participants will have an opportunity
to share industry best practices to tackle validation
challenges.
This event is
not-to-be-missed, and it’s FREE of charge!
Where?
POINTE-CLAIRE-MONTREAL AEROPRT
6700 TRANS CANADA
HWY
POINTE CLAIRE, QC H9R1C2, CANADA
1-514-697-7110
To RSVP Contact: OR
Abigail Oti-Yeboah, BBA
T: (905) 738 3773 x 2230
E: aotiyeboah@complianceassociates.ca |
