Regulatory Focus™ > News Articles > Health Canada Updates CGMP Guidance for Biologics and Blood Products

Health Canada Updates CGMP Guidance for Biologics and Blood Products

Posted 12 November 2012 | By Alexander Gaffney, RAC

Health Canada has updated its current good manufacturing practices (CGMP) guidelines for Schedule D (biological) drugs and human blood and blood components.

The updated guidance covers 13 distinct areas of CGMP compliance:

Premises: Sets recommendations for manufacturing facilities, including screening areas for blood donors, secured quarantine storage and handling areas, separate areas for testing biological samples and storage requirements.

Equipment: Sets recommendations for laboratory testing equipment, water purification systems, equipment validation and maintenance, equipment used for specific procedures, the safety of collection procedures and the validation of computers used to maintain patient data.

Personnel: Sets recommendations for managerial authority, staff training, staff qualifications, continuing education, key staff roles and educational requirements.

Sanitation: Sets recommendations for the maintenance of a clean and sanitary manufacturing facility, the establishment of safety procedures, personnel control and hygiene and sanitary procedures for staff.

Raw Material Testing: Sets recommendations for donor screening and vendor audits.

Manufacturing Control: Sets recommendations for operating procedures, document control, the documentation of all significant operational steps, document change control procedures, supply and reagent controls, component labeling, recall procedures and audits.

Quality Control Department: Sets recommendations for the personnel makeup of the facility's quality control department and operations, including the formation of a quality control program.

Packaging Material Testing: Sets recommendations for the use of approved blood product collection and satellite bags-both of which are approved as medical devices through a separate process and do not require further testing.

Records: Sets recommendations for record keeping, including legibility and content.

Samples: Sets recommendations for transfusion samples, which much be stored in a frozen state if stored long-term.

Stability: Sets recommendations for storage and shipment.

The new guidance supersedes a 1999 version, and came into effect on 9 November 2012.


© 2021 Regulatory Affairs Professionals Society.

Regulatory Focus newsletters

All the biggest regulatory news and happenings.