SIRO ClinPharm Partners with European Regulatory Expert
Indian CRO SIRO Clinpharm partnered with UK-based regulatory consulting firm Cambridge Regulatory Services (CambReg) to offer full regulatory services to clients conducting clinical trials in Europe. Services include the preparation of clinical trial applications, marketing authorizations, specialist paediatric investigation plans and paediatric use marketing authorizations.
SIRO Clinpharm has European offices in Germany, Romania, Estonia, Greece, Czech Republic and Spain, as well as offices in India, the U.S., Israel, and Europe.
"Our alliance with CambReg would go a long way in helping small and mid-sized companies cut through the regulatory maze in Europe" said SIRO Clinpharm’s chief operating officer, Chetan Tamhankar, in a statement. "This alliance builds on the strength of our European clinical trial operations and allows us to offer greater value to our clients."
CambReg offers regulatory compliance advice and submissions services to clients in Asia, Europe and the U.S.