Services Overview

Clinical Trials

Regulatory

Medical & Pharmacovigilance

Nonclinical Safety

Data Management & Biostatistics

Chemistry, Manufacturing and Controls

Medical Writing

Quality Assurance

Project Management

Investigator Registry

Services: Regulatory

Cato Research has the expertise to devise successful regulatory strategies and to prepare or review relevant regulatory documentation for the pharmaceutical, biotechnology, and medical device industries. Additional services include assisting in compliance audits, licensing activities, and regulatory training. Cato Research also offers a regulatory database and system for handling the sponsor's regulatory files, useful for project status reports and inventories of auditable documents, which is much needed during study conduct and regulatory inspections.

Cato Research regulatory personnel are highly experienced in multiple areas and have gained Regulatory Affairs Certification from the Regulatory Affairs Professinals Society (RAPS).