The RAPS store will be under maintenance Saturday, 28 September between 6 a.m. and 12 p.m. Store functionality may be unavailable at times during this window.
We apologize for any inconvenience caused during this time.
EAS Consulting Group, LLC (EAS) specializes in Food and Drug Administration (FDA) regulatory matters. Our focus is to assist domestic and foreign pharmaceutical, medical device, tobacco, food, dietary supplement, and cosmetic firms comply with applicable laws and regulations. EAS is staffed with former FDA compliance and inspection officials, and has an extensive network of consultants with many years of FDA and industry experience.
Headquartered in Alexandria, VA with consultants and auditors located strategically throughout the U.S., EAS was established as an independent company in October 2006. Prior to that, it was a division of Kendle Regulatory Affairs.
1700 Diagonal Road, # 750
Alexandria, Virginia 22314
President & COO
Director Reg Info/Submissions
|Professional Responsibility (Regulatory Process):
||Good Laboratory Practice (GLP)
Quality System (QS)
Good Clinical Practice (GCP)
Good Manufacturing Practice (GMP)
Biological License Approval (BLA)
Investigational New Drug (IND)
Investigational Device Exemption (IDE)
New Drug Approval (NDA)
Premarket Approval (PMA)
Premarket Notification (510k)