background image for GxP Lifeline
GxP Lifeline

Creating, Staffing and Managing an Inspection War Room


Note: The views expressed in this article are those of the author and do not necessarily represent those of his employer, GxP Lifeline, its editor or MasterControl Inc.


When I served in the military there was a term used that is still pretty familiar today: "sound general quarters!" When this order was issued, everyone instinctively stopped what they were doing and manned whatever station was theirs during that time. All commands during general quarters came from the war room behind the bridge of the vessel.

Many companies in the life science sector hear their own version of "sound general quarters!" from FDA and anxiously await the ultimate examination: An inspection visit by the FDA. One of the key components of hosting such an inspection is the preparation and use of a "war room" during the visit. It can be referred to as the primary line of defense in the success of such a visit.

This strategic office should be devoted and organized to provide the necessary objective evidence requested during such an inspection. One of the key observations the inspector will make is the timeliness of the turnaround of a request. A speedy response is always favorably acknowledged and a well-organized war room makes that possible.

One of the key components of hosting such an inspection is the preparation and use of a "war room" during the visit. It can be referred to as the primary line of defense in the success of such a visit.

War Room Components

Three war room components should be easily accessible during the inspection: desktop documentation; records of data and recorded information; and pre-selected auditees and their backups.

Making these items quickly available requires some pre-planning. Choose a war room location in an office area that is not in the traffic mainstream. It should be in close proximity to the room hosting the inspection. All electronic venues should be available, including email, cell phone and a reliable devoted printer (e-documentation). Be cognizant of the nature of documents to be made available in terms of sign-offs for review and approvals of documents and records . Conducting a dry run for war room readiness as part of a mock audit would be very prudent.

Pre-selected auditees should be "processed" through the war room before entering the "inspection arena." Coaching in the war room before entering an inspection interview will be very effective in setting the appropriate tone for the auditee. Also, if last minute plans for availability change, then the war room can regroup, preparing the backup auditees before the inspector's interview.

The strategic person in the war room should have certain items at their finger tips at the start of the inspection:

  • A quality system manual and/or site master plan
  • An organization chart showing the relationship of quality and regulatory management
  • Key SOPs that manage quality and compliance system: CAPA, record control, internal audits, change control, master batch or actual batch records and associated process flow diagrams
  • Permissions for file access, or person(s) who can access critical information when "on-deck"

This inspection moment for a company should be a call to "general quarters" but the war room should be prepared under the motto "Semper Paratus," meaning always ready. When the call to duty comes, everyone should know their positions. All will await the orders from the war room while the company continues to navigate its business affairs. No one should be lackadaisical until the order comes to "stand-down" from the war room.


Walt Murray is a quality management and regulatory affairs professional with more than 32 years working with internationally recognized and highly-regulated companies, including J&J, Merck, Pfizer, Stryker, USANA and Del Monte Foods. A Six Sigma Black Belt, Murray is certified (CSSMB) in quality and environmental systems auditing (RAB/QSA/IATCA/IRCA), critical-thinking skills (CTS Facilitator) and process control (SPC/SQC). Having personally performed more than 350 1st/2nd/3rd-party audits for a variety of Fortune 500 life sciences companies, Murray has hosted investigational and systems audits by the FDA, Therapeutic Goods Administration (TGA), Medicines and Healthcare Products Regulatory Agency (MHRA) and Health Canada (CMDR). Walt is based in Salt Lake City, Utah, and works as an independent expert as he supports regulated clientele for GMP, GLP, IVD, GCP and the cross-disciplinary development of MDSAP companies.


[ { "key": "fid#1", "value": ["GxP Lifeline Blog"] } ]