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. The Company's new headquarters is at 583 Mountain Avenue, North Caldwell, New Jersey 07006. The Company has affiliates in many cities around the world including Toronto, Heidelberg, London, Osaka, Paris, Rome, Taipei, Beijing, and Warsaw.
© 2010 Schiff & Company 583 Mountain Avenue, North Caldwell, New Jersey 07006 | (973) 227-1830