About The Auditing Group   856-437-5880

For Audits, Remediation or Gap Analysis servers, please fill out the Contact form and an SME will contact you.

  • Audits - GMP/GLP/GCP Auditing – Vendors/Suppliers, QMS, GMP Process, Equipment, Facilities, Laboratory, Software, & Validation: 

  • GMP requirements supporting Bio-Pharmaceutical – API / Excipients

  •  Medical Device Audits – QMS Remediation, ISO 13485, Class I, II, & III, Combination.

  •  GMPs for the Cosmetic Industry. 

  •  Good Laboratory Practice requirements supporting laboratory and testing services. Including GCLP.

  •  Good Clinical Practice requirements supporting clinical activities. Supporting GCLP.

  •  ‘For-Cause’ and ‘Due-Diligence’ audits.

  • Quality Management Systems Audits - Medical Device Industry (FDA / EMeA / ISO) 

  • Electronic Systems and Software Audits (21 CFR Part 11 / EU Annex 11) 

  • Validation and Qualification Audits

The Auditing Group

US Offices:

​

Southampton, NJ

Physical Address: 4 Linda Lane, Suite B, Southampton, NJ 08088

Mailing Address: PO Box 1696

Medford, NJ 08055

​

Sarasota Florida

Physical Address: 5377 Trails Bend Court, Sarasota, FL 34238

Mailing Address: The Auditing Group, PO Box 268, Ospry, Florida

​

Asia - Pacific Office: 

Room 215, A2 floor, No. 218 Xinghu Street, Suzhou City, Jiangsu Province

​

​

​

GMPLogos150.jpg
TAG211126-150.jpg
GMPBCLogo8-800.jpg

Contact Us to Receive a Turn-key Quote!

Location of Service:

Other Country:

Select Service Types Below:
Select The Industry

GMP, GLP, GCP, US FDA,EU EMA, ISO, Audits supporting:​