Good Manufacturing Practices (GMP)

Both the Drug Regulations and the NHP Regulations have specific requirements for Good Manufacturing Practices (GMPs). Both frameworks outline basic requirements for drug and natural health products (NHPs) GMPs within the regulatory framework. More detailed requirements or expectations are then published in various interpretative guidelines.

The goals of GMP are to establish the following:

• Ensure that drugs and NHPs are manufactured, packaged, labelled, tested, or stored in an environment which does not compromise the product’s safety or efficacy.
• That personnel with adequate training and expertise are available to carryout, supervise or approve various GMP activities.

DSA Consultants offers a full range of GMP Consulting Solutions related to:

• Establishment Licenses
• Validation, Mapping, Cold Chain Packaging and Qualification
• GMP Audits
• Standard Operation Procedures
• GMP Training

Contact us to find out more about GMP Consulting Solutions or to receive a free copy of our white paper on marketing a healthcare product in Canada, click here.