Pharmaceutical Quality Control & Assurance Software Systems

As pharmaceutical companies seek to manage a competitive market and FDA regulations, MasterControl Inc. provides pharmaceutical quality control & assurance software systems for automating quality processes.

The right pharmaceutical quality assurance software plan can spell out success for FDA-regulated companies seeking the peace of mind sustained regulatory compliance can bring.

While the FDA encourages modernization and harmonization with other quality system requirements, the agency is also required to ensure that pharmaceutical quality assurance software includes compliance with CGMPs (21 CFR Parts 210, 211) and electronic system requirements (21 CFR Part 11).

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Interactive and Live Demonstration: MasterControl Quality Suite Demonstration
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White Paper: Six Ways to Optimize Your Quality Management System and Ensure FDA and ISO Compliance
White Paper: Six Corporate Oversights of Quality and Compliance Issues in Pharmaceutical Environments
Q&A: New ICH Q10 Harmonization Guidance for the Pharmaceutical Industry
Case Study: Teva Pharmaceuticals



Q&A Session on Pharmaceutical Quality Control Software Systems

The Q&A session based on the FDA's Quality Control Systems Approach to Pharmaceutical cGMPs addresses topics related to the Guidance for Industry Pharmaceutical Quality Control Systems Approach to cGMP Regulations and answers the following questions:

  • Who is covered in the guidance?
  • What is the Six-System Inspection Model?
  • What is the Quality Systems Model?
  • What's the connection between this FDA guidance and MasterControl software?
  • What are some of the MasterControl pharmaceutical quality control software features and how do they relate to this FDA guidance?

Pharmaceutical Quality Assurance Software Systems - Industry Experience and Innovation

MasterControl Inc. is leading global provider of web-based process and document management software solutions and helps regulated companies sustain regulatory compliance with an unmatched combination of industry experience and innovation.

MasterControl's pharmaceutical quality assurance software system offers complete solutions to solve the challenges of regulatory compliance. Knowledgeable MasterControl representatives can help each company decide on the specific software that is right for them, and can then configure a complete QA software plan that meets their unique needs.

Configuring the Pharmaceutical Quality Control Software Solution

The solutions that lie within any pharmaceutical quality assurance software plan include the latest technology and the organizational know-how to make any FDA regulated company's day-to-day processes more efficient and effective. MasterControl's Pharmaceutical Quality Control & Assurance Software include the following:

MasterControl Pharmaceutical Quality Assurance Systems

For pharmaceutical companies, MasterControl can provide an array of web-based pharmaceutical quality assurance software systems that automate, streamline and funnel quality processes, quality documentation and CAPA controls into a fast and effective quality management system. The system includes the control of quality assurance (QA) processes such as audits, deviations, nonconformance, change control, CAPA, etc. To learn more about automating a Total Quality Management (TQM) system please feel free to contact a MasterControl representative.

Pharmaceutical Quality Control Software System Exceeds Expectations

MasterControl, Inc., a developer of software solutions, provides more than the technology for pharmaceutical quality control. MasterControl's solutions address the needs of all departments within ISO-standardized and FDA-regulated companies from engineering to quality, and from development to regulatory. To learn more about MasterControl's pharmaceutical quality control software systems for faster speed-to-market and surer compliance, please feel free to contact a MasterControl representative.


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