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How do biotech firms benefit from working
with us? The answer is obvious: save time and money
and improve your chances of success. Optimally, we begin
to help at the non-clinical stage with scientific and
regulatory planning and advice. This enables clients
to get value from the start. We can be called upon periodically
during the development process for many reasons including
regulatory consultation, clinical protocol and Investigator’s
Brochure (IB) preparation, submission preparation, interaction
with regulatory authorities, and advising on setting
and meeting regulatory requirements, and planning and
executing US penetration. We always keep foremost in
mind the goal of streamlined drug development ending
with approval and optimal product labeling.
“Engaging a service provider should be considered
if it is likely that the job will be done less costly,
more efficiently, and with a higher chance of success
than if you were to do it yourself”
Location
We are situated in the Children’s Hospital of
Eastern Ontario Research Institute, in Ottawa, Canada’s
capital city. This places us at the heart of Canada’s
medical science community and close to the federal regulatory
decision-making body. Our location in an extensive health
sciences campus provides ready access to scientists,
investigators, and patient populations.
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