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 8,000 protocols spanning virtually every therapeutic area; an IRB that has passed dozens of customer audits and was accredited in 2005; 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.