Why Schulman?
If you prefer to work with a central IRB that has built a reputation since 1983
for performing high quality reviews in a timely manner; an IRB that has been selected
by virtually every major pharmaceutical and biotech company to perform reviews of
their studies; an IRB that repeatedly works with all of the top CROs; an IRB that
has reviewed nearly 10,000 protocols spanning virtually every therapeutic area;
an IRB that has passed dozens of customer audits; an
IRB that has not received a Form 483 after any of its last three FDA audits.
If you prefer to work with a central IRB that is constantly seeking new and better
ways to serve its customers; if you prefer an IRB that is committed to getting it
right, and equally committed to fixing it if something goes wrong - regardless of
the reason, then you have finally found the IRB for which you have been looking.
Schulman Associates IRB - Exactly what you're looking for in an
IRB.