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Quality Systems

Therapure Biopharma is committed to quality in every aspect of its operations – our duty is to ensure that your products meet all quality, safety and efficacy requirements. Our Quality Assurance team is highly experienced in quality control processes and we ensure that only approved and qualified vendors are used and that audits are conducted regularly.

Working from our dedicated 5,800 sq. ft. laboratory, our Quality Control group meets both our clients’ high standards and cGMP compliance. Our validation expertise extends from in-product testing and product release to Process/Performance Qualification (PQ) of many typical bio/pharmaceutical operations such as viral clearance, filtration/clarification, purification, aseptic filling and scale-up operations. We also possess in-depth knowledge and the ability to address process cleaning validation requirements.

Please find below an example of the Therapure Quality Agreement and Quality Charter which are tailored to each clients needs

 

Quality Agreement
Our Quality Agreement Our Quality Charter

 We understand the discipline required to ensure the product quality attributes are maintained and documented.You can trust our quality systems to ensure that your product meets all regulatory needs.

tel: +1 (905) 286-6200
info@therapurebio.com

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