Differences Between 21 CFR Parts 210 and 211
While 21 CFR Parts 210 and 211 both apply to GMP of drug products, each part addresses a different set of guidelines.
- Part 210 – Outlines the minimum GMP requirements covering manufacturing, facilities, and controls for the manufacture, processing, packing, and holding of all drugs in a way that meets the guidelines for safety, quality, and purity.
- Part 211 – Outlines the minimum GMP requirements for finished drug products. Part 211 also covers various other areas, including personnel, facilities and equipment, production processes, stability testing, and labeling.
21 CFR Parts 210 and 211 Requirements
Subpart F, Section 211.100 – There shall be written procedures for production and process control, assuring that drug products have the intended identity, strength, quality, and purity. Written procedures, including any changes, shall be drafted, reviewed, and approved by the appropriate organizational units.
Subpart I, Section 211.160 – Any changes in specifications, procedures, sampling plans, or other laboratory control mechanisms shall be documented at the time of performance and reviewed by the appropriate organizational units.
Subpart B, Section 211.25 – Each person engaged in the manufacture, processing, packing, and holding of a drug product shall have the necessary education, training, and experience to perform the assigned functions.
Subpart J, Section 211.198 – Written procedures describing the handling of all written and oral complaints regarding a drug product shall be established and reviewed by the quality control unit.
Corrective and Preventive Action (CAPA):
Subpart J, Section 211.192 – Any unexplained discrepancy or the failure of a batch or any of its components to meet any of its specifications shall be thoroughly investigated. A written record of the investigation shall be made and shall include the conclusions and follow-up actions.
Subpart J, Section 211.180 – All records, or copies of records, shall be readily available for authorized inspection. Records shall be subject to photocopying or other means of reproduction as part of such inspection. Records that can be immediately retrieved from another location by computer or other electronic means shall be considered as meeting this requirement.
Subpart E, Section 211.84 – Each component shall be tested for conformity with all appropriate written specifications for purity, strength, and quality. Any lot of components that does not meet the specifications shall be rejected.
Staying Compliant and Connected
Compliance with the 21 CFR guidelines for pharma requires efficient management of disparate GMP functions to ensure drug products meet the requirements for safety, quality, strength, and purity. Automating quality and manufacturing management is the most effective way for pharmaceutical companies to collaboratively manage all aspects of drug product development.
MasterControl’s Quality Excellence™ solutions integrate all quality and manufacturing processes, making it easier to achieve compliance with all 21 CFR 210 and 211 requirements, including documentation, changes, training, complaints, CAPA, audits, and nonconformance.
MasterControl Solutions Specific to 21 CFR Guidelines
Achieving compliance with 21 CFR Parts 210 and 211 requires strict attention to all of the GMP requirements. MasterControl equips you with all of the necessary tools to successfully meet the regulatory guidelines:
- MasterControl Documents™ – Automates routing, version updates, approvals, and distribution. It stores all documents in a secure, central repository for easy search and retrieval.
- MasterControl Change Control™ – Automates every step of the change control process, from submission through implementation, verification, and end of lifecycle.
- MasterControl Training™ – Streamlines and increases the efficiency of training management tasks, from routing and tracking to follow-up and escalation.
- MasterControl Customer Complaints™ – Provides a secure and centralized platform for receiving customer complaints, organizing data, and storing documents for easy correction of issues.
- MasterControl CAPA™ – Streamlines all CAPA tasks, including data gathering, routing, escalation, and approval for more efficient and accurate CAPA management.
- MasterControl Audit™ – Improves efficiency of audit planning and preparation, capturing findings, and creating customizable audit reports.
- MasterControl Nonconformance™ – Automates the processes for identifying, evaluating, reviewing, and handling nonconforming materials, components, parts, and finished products.
How to Achieve 21 CFR Compliance With MasterControl
More companies are discovering that achieving compliance with 21 CFR Parts 210 and 211 is easier using automated technology. MasterControl’s Quality Excellence™ solutions have functionality that directly aligns with all of the GMP guidelines. Other benefits of using MasterControl include:
- Unified platform – A fully connected and collaborative organization is essential for regulated companies. MasterControl integrates all quality and manufacturing management applications, processes, data, analytics, reports, and document control tasks on one centralized platform.
- Risk management – MasterControl Risk™ unifies all risk-related activities for a more complete and accurate picture of the risk landscape across business units, processes, and products.
- Accelerates compliance – Increases operational efficiency, improves product quality, and speeds time to market.
- Scalable – flexible solutions meet the needs of companies of every size.
QMS Provider for the FDA
MasterControl Inc. and its partner company, i4DM, have been the QMS providers for the FDA’s Office of Regulatory Affairs (ORA) since 2009. The FDA recently expanded its implementation of MasterControl’s Quality Excellence™ solutions to improve the quality and audit management processes of the Division of Pharmaceutical Analysis in the Center for Drug Evaluation and Research (CDER).