Pre-Health Authorities Mock Audit

• GMP Audit
• GXP Audit
• Third Party / Vendor Audit
• Pre-Health Authorities Mock Audit
• Warning Letter Lifting
• Post Inspection Remediation
• Import Alert Lifting
• Quality Systems Development
• Computer System Validation
• Merger and Acquisition Consulting Services
• GMP Retainership on Hourly Basis
• Quality, GMP and Technical Trainings
• Engineering Services
• SOP Review and Writing
• Upgradation of Domestic Site to Regulatory

A Pre-Health Authorities Mock Audit in the pharmaceutical industry refers to an internal review process conducted by a pharmaceutical company to assess its compliance with regulatory requirements before an official inspection by health authorities, such as the FDA (Food and Drug Administration) in the United States, EMA (European Medicines Agency) in Europe, or other national regulatory bodies. MASUU performs the mock audit to identify and rectify any potential compliance issues to ensure readiness for the actual regulatory inspection. MASUU GMP team, which was trained by former Agency personnel from FDA, MHRA, EMA, ENVISA, TGA, ENVIMA…etc, helps in Regulatory Readiness, Ensures the company is well-prepared for actual health authority inspections, reducing the risk of regulatory action such as warnings, fines, or product recalls. By conducting a thorough Pre-Health Authorities Mock Audit, pharmaceutical companies can proactively manage compliance, enhance their quality systems, and ultimately safeguard patient health.