One standard of rigor.
A global perspective.
COTA is based in the United States and collaborates with international study teams and partners. We help align scientific, programming and reporting work across organizations and jurisdictions.
NOT LIMIT EXPERTISE.
Working across
time zones and teams.
Modern clinical development is international by default. Studies may involve multiple sites, CRO partners, regulatory expectations, and data-management functions across borders.
COTA can collaborate as a focused specialist partner within sponsor- or CRO-led governance, with clear handoffs, working agreements and communication channels.
Discuss an international program ↗Different regions. Shared scientific discipline.
FDA
United States drug and medical device regulatory resources.
EXPLORE REGULATOR ↗EUEMA
European medicines evaluation and related scientific guidance.
EXPLORE REGULATOR ↗UKMHRA
United Kingdom medicines and medical-device regulation.
EXPLORE REGULATOR ↗GLOBALICH
International harmonization of technical requirements for pharmaceuticals.
EXPLORE REGULATOR ↗Good science deserves
great execution.
Bring us the question, the protocol, or the challenge. We'll help map the next move.