Mock Audit services are offered by a collaboration of experienced, independently successful CGMP Quality consultants. The team assembles the requisite skill sets for the particular job and can handle the largest facility audit or the start-up who wants a quick review prior to the Agency visit.
Identify the deficiencies in your Quality CGMP in time to work on them before the FDA arrives.
This team provides a comprehensive review and audit process to assist manufacturers of Pharmaceuticals, Bio-tech, Medical devices, Oral dose, Inhalation and Nanotechnology related companies to meet regulatory standards in pre-approval (PAI) and other licensing inspections for US and International compliance.
The team is comprised of 4 experts that represent over 100 years of experience in their related fields.
Over 35 years of experience in cleanroom design, gowning maintenance, and qualification; controlled environment management; GMP compliance and training; and contamination control.
Over 40 years of experience in facility and basis of design (BOD) for pharmaceutical and biotechnology plants; HVAC and WFI systems design, utilities and process equipment validations and PM programs; expert operations management.
Over 30 years in contamination control measures (sterile, aseptic and non-sterile manufacturing); environmental monitoring; sanitizers/disinfectants qualification; GMP compliance and training; and QC microbiology laboratory testing and operations.
Over 27 years in pharmaceutical development with a focus in biopharmaceutical regulatory affairs; quality systems auditor; analytical methods development and validation; comparability; and change control.
This team is experienced in reviewing all production and support facilities and utilities, validation, testing and all finished product documentation.
Our expert comprehensive review balances the time on-site, report of findings, and if needed, corrective action SOLUTIONS that will assist the client is a successful inspection. This cost-effective direct approach helps our clients experience a successful inspection and license. By using a structured review of the production facilities, utilities, validation, testing and other manufacturing documentation, the PAI Team makes the most efficient use of on-site auditing, report writing, and if requested, corrective actions.
Take advantage of the extraordinary breadth of skills offered by this experienced team with seasoned, proven advice. In addition to the mock audit and PAI preparation services, this team is available for: