U.S. FDA Regulations & cGMP Software
The U.S. FDA's regulations for pharmaceutical, medical device, blood and biologics, and other regulated industries embody the cGMP principles that are widely followed throughout the world today. These regulations are also the basis of cGMP software available in the market today. The FDA's 21 CFR Parts 210-211, which apply to pharmaceutical companies, are a good example of how cGMP principles help ensure product quality and consumer safety. The regulations cover every aspect of drug development and manufacturing, from personnel to processes to distribution. Likewise, a cGMP system must cover all of those aspects for compliance purposes.
The FDA took its cGMP initiative further when it released the "Pharmaceutical cGMPs for the 21st Century: A Risk-Based Approach" in 2002. The initiative examined cGMPs as they applied to modern technological advances in the pharmaceutical industry. It was also meant to harmonize the FDA's efforts on quality improvement with its international counterparts. The risk-based approach has since become the basis of cGMP software solutions widely used in the industry today.
ISO Quality Guidelines & cGMP Software
ISO quality standards are used by general manufacturers throughout the world. These standards are designed to ensure product quality and processes, just like the cGMP regulations enforced by the FDA. However, they differ in their target audiences and specific requirements. Companies that comply with both FDA rules and ISO standards must develop a cGMP system that addresses both.
For medical device manufacturers, there is an overlap in cGMP and ISO requirements. ISO 13485:2003 is a quality standard that applies to medical device companies. 21 CFR Part 820 (Quality System Regulation or QSR) is the GMP regulation for medical device companies enforced by the FDA. The FDA has harmonized QSR with ISO standards, making them complementary. In looking for cGMP software, companies should make sure that the solution they choose addresses both GMP and ISO 13485 standards.
Compliance with the Help of MasterControl's cGMP Software
MasterControl quality and compliance software addresses cGMP requirements and is widely used by regulated companies as cGMP software and platform for a compliant cGMP system.
MasterControl's cGMP software can automate all quality processes critical to compliance, including document control, change control, CAPA, training management, and audit management, among others. Here are some of the benefits of using MasterControl as the foundation of your cGMP system:
- Automation and Standardization: With MasterControl's cGMP software, you can standardize all documents-based processes and automate distribution/routing, review, follow-up, escalation, and approval of documents. It makes search and retrieval of documents faster and easier.
- Centralized Platform: MasterControl can serve as a centralized platform for all quality documents and records critical to cGMP compliance, making it essentially your cGMP system. MasterControl is web-based so authorized users have access to the system from virtually anywhere 24/7.
- Connectivity: MasterControl is unlike other cGMP software solutions in the sense that it can connect all quality processes, including document control, training control, audit management, nonconformance management, CAPA, and change control. This connectivity will help ensure that quality and other issues will not fall through the cracks.
- Mobile Access: With MasterControl, users can access the system using a tablet or a smartphone. This capability is a distinct advantage of MasterControl over other cGMP software solutions and it can be very helpful for users out in the field or those constantly traveling. Those users will be able to participate in documents-based processes critical to cGMP compliance even when they are not in front of their computers in the office.
For More Information on MasterControl's cGMP Software Systems
To learn more about MasterControl's cGMP software systems, contact a MasterControl representative.