Quality Assurance (QA)
Supporting a wide range of Pharmaceuticals by Complying to Health Canada GMP regulations; including but not limited to Biologics (Schedule D), Prescription (Rx) medication, OTCs and NHPs.
1
Quality System Implementation and Maintenance
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Development of QMS: Creating Quality Management Systems compliant with Canadian regulations.
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QMS Maintenance: Ongoing support to improve and maintain existing QMS.
2
Batch Record Review and Product Release
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Manufacturing and Packaging Review: Detailed review of batch records to ensure compliance.
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Product Quality Review: Ensuring products meet quality standards before release.
3
GMP Audits Support
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Internal and Vendor Audits: Comprehensive GMP audits for internal processes and external suppliers.
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GMP Training and Certification: Training programs to ensure compliance with GMP standards.
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GMP Documentation: Development and review of SOPs and other GMP-related documents.
4
Documentation Services
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Quality Document Creation: Development of SOPs, work instructions, and quality agreements.
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Document Control and Management: Efficient management of quality documentation.
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