Quality Assurance
Quality is at the very centre of everything we do

Our GMP guidelines provide a system of processes, procedures and documentation to assure that the product manufactured has the identity, strength, composition, quality and purity that appear on the product label.

At Pharmaline, quality assurance program is extensive and we are committed to ensuring always the highest quality, most efficacious and unquestionably pure and safe products.

Pharmaline’s Quality Assurance Program involves the following key components:
  • Vendor Qualification
  • Ingredient Testing
  • In-Process Testing
  • Finished Product Testing
  • Document Control
  • Record Retention
  • Regular Quality Audits

Pharmaline implements a comprehensive set of Standard Operating Procedures (SOPs) in accordance with Good Manufacturing Practices (GMP) and the requirements of Canadian and international regulatory bodies. We strictly adhere to the SOPs to maintain consistency in every step of the manufacturing process. SOPs are regularly reviewed and updated as necessary to ensure that procedures are modified when changes are made to equipment or processes.

All products are made to strict manufacturing standards and quality is checked along the manufacturing process, and finished product testing is conducted at certified thirdparty testing laboratories



address

UNIT 5
2835 ARGENTIA ROAD
MISSISSAUGA ON,
CANADA L5N 8G6

OFFICE HOURS

Mon - Fri: 8am to 5pm
Sat & Sun: Closed

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