Do
you want to make a difference?
If you're a healthy, non-smoker,
18+ years of age, contact Biovail Contract
Research and inquire about participating
in a clinical study. Biovail tests generic
equivalents and/or modified versions
of established medications.
Safety & Precautions
Biovail Contract
Research takes many precautions before
and during any given study. All participants
must undergo an Informed Consent procedure,
during which they are informed of
their rights and obligations, potential
side effects and other study details.
An Institutional
Review Board (IRB) reviews a protocol
that outlines the study and provides
explicit details of any known potential
side effects. The IRB is comprised
of a group of doctors, pharmacists
and other community members whose
primary objective is to ensure the
safety of all participants.
All studies adhere
to strict guidelines regulated under
the U.S. Food & Drug Administration
(FDA), and the Therapeutics Products
Directorate (TPD) in Canada.
For more information
regarding forthcoming studies and
compensation, click
here.
|
