Quality
Quality is of the utmost importance at Uman Pharma. Manufacturing and distribution processes are fully validated. Documentation is maintained to ensure product traceability. Both manufacturing processes and products are controlled.
Quality Assurance
The Quality Assurance group is responsible for maintaining effective quality systems (including thorough documentation) to ensure that every product or service meets specified requirements.
GMP practices at Uman Pharma require that all manufacturing and testing equipment has been qualified as suitable for use, and that all operational methodologies and procedures (such as manufacturing, cleaning and analytical testing) utilized in the drug manufacturing process have been validated.
Quality Control
The group responsible for coordinating the quality control activities associated with manufacturing activities follows a set of procedures intended to ensure that manufactured products or manufacturing support activities adhere to predefined sets of quality criteria or requirements. The Quality Control group’s responsibilities cover all activities including design, development, documentation, production and inspection processes. It includes the quality control of raw materials, components and finished products.
This group comprises analytical and microbiological lab personnel, line inspectors, auditors and document reviewers.
100, de l'Industrie Boulevard, Candiac, Québec, Canada, J5R 1J1
(450) 444-9989 / 1 877 444-9989
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