Pharmaceutical, Biological and Device Regulatory Affairs, Compliance, and Clinical Trials
Company, Inc., founded in 1982, specializes in full services to the
industries regulated by the United States Food and Drug Administration (FDA) and
similar agencies in other countries. Services provided include the preparation
of regulatory filings, the planning and conduct of clinical studies, and
the evaluation of compliance with standards of Good Manufacturing
Practice (GMP), Good Clinical Practices (GCP)
and Good Laboratory Practices (GLP). Schiff &
Company has extensive experience with drugs, biologics, medical devices,
foods, dietary supplements, and cosmetics.
Schiff & Company, Inc. provides regulatory consulting services to the pharmaceutical industry in both the United States and foreign countries. In 1990 the company moved to larger offices at 1129 Bloomfield Avenue in West Caldwell, New Jersey. At the beginning of 2013 the company moved to its present suite of offices at 1120 Bloomfield Avenue. The company has affiliates in many cities around the world including Toronto, Heidelberg, London, Osaka, Paris, Rome, Taipei, Beijing, and Warsaw.
© 2010 Schiff & Company 1120 Bloomfield Avenue, Suite 103, West Caldwell, New Jersey 07006 | (973) 227-1830