Consulting

Clarmon guides companies in developing and implementing GMP compliance strategies, assisting them with FDA pre- and post-approval inspections, QA/QC documentation review, regulatory interpretation and submissions.

As appropriate and according to client needs, we perform internal audits and general GMP compliance auditing. Audits are tailored to meet the specific requirements of your company, and help achieve compliance with regulatory requirements in the most efficient way appropriate.
Clarmon can also assist your company in the development of GMP Quality Systems.


We also provide consultancy in:

• Compliance Reviews and Audits
• Master Validation Plan (MVP / VP)
• User Requirement Specifications and Functional Specification (URS / FS)
• Design and Installation Qualification (DQ / IQ)
• Operational and Performance Qualification (OQ / PQ)
• Validation within Equipment, Process, Cleaning and Computer Systems
• Standard Operating Procedure (SOP)