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Quality Systems and Quality Management

What is Pharmaceutical Quality Management?

Compliance to current Good Manufacturing Practices (cGMPs) is critical to your business, your patients, and the expectations of the Food and Drug Administration (FDA). Today’s pharmaceutical and medical device manufacturing is complex and requires significant experience in GMPs to ensure compliance. Ensuring your Contract Manufacturing Organization (CMO) or Contract Laboratory Organization (CLO) meets or exceeds FDA regulations is a must in today’s highly regulated environment. To comply with the FDA’s requirements under 21 CFR parts 210, 211, 820, and 11, you must have robust quality systems and processes, and a well-defined supplier qualification process. ProPharma Group has the expertise and industry experience to perform and manage these processes for your organization.

ProPharma Group: Your Trusted Partner for Pharmaceutical Quality Systems

ProPharma Group will work with you to make sure all processes are compliant by conducting a Quality Gap Analysis or performing independent GMP audits. Whether your challenge is with manufacturing, packaging, aseptic processing, laboratory investigations, labeling, validation, Standard Operating Procedures (SOPs), training, corrective and preventive actions (CAPAs), product adulteration, raw materials storage, risk management, or other quality issues, we can provide the quality operations, quality systems, and manufacturing expertise required to help you prevail.

Our experts will spend significant time on-site at your facility examining all aspects of your quality systems and manufacturing operations. We will work with your organization and review the following:

  • Personnel Qualification and Staffing
  • Quality Manual
  • Change Control
  • Deviations
  • Investigations
  • CAPAs
  • Document Management
  • Electronic Quality Management Systems
  • Process Validation
  • Cleaning Validation
  • Equipment Qualification and Validation
  • Manufacturing Batch Records
  • Packaging Batch Records
  • Part 11 Compliance
  • Laboratory Controls
  • Analytical Method Validation
  • Supplier Qualification Program
  • Internal Audit Program
  • Raw Material Testing and Controls
  • Environmental Monitoring
  • Inventory Management
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