Ensuring Quality From Process to Product
At Dr. Raza Pharma, the Quality Assurance Department ensures that quality is integrated into every stage of pharmaceutical manufacturing — from raw material approval to final product release.
Our QA systems focus on maintaining controlled processes, effective documentation, regulatory compliance, and continuous improvement to ensure that every manufacturing activity follows approved procedures and established quality standards.
Through strong systems, professional expertise, and continuous improvement, we are committed to delivering pharmaceutical solutions that healthcare professionals and patients can trust.
Quality Assurance Department
The Quality Assurance Department at Dr. Raza Pharma is responsible for establishing, monitoring, and maintaining effective quality systems across the complete pharmaceutical manufacturing lifecycle.
QA ensures that all operations are performed according to approved procedures, documented processes, Good Manufacturing Practices (GMP), and applicable regulatory requirements.
Role of Quality Assurance
Reviewing and approving materials before use
Checking production areas, equipment, and documents before manufacturing
Monitoring process controls and hygiene practices
Ensuring compliance with approved SOPs
Reviewing batch manufacturing records
Supporting documentation accuracy and traceability
Coordinating corrective and preventive actions where required
Ensuring proper review before product release
After Production
After completion of manufacturing, QA performs a detailed review of batch documentation, quality records, and relevant production information before final product release.
This process ensures that every batch has been manufactured according to approved standards and meets defined quality requirements before reaching the market.
No product is released without completing the required quality review and approval process.
Documentation, SOPs & Compliance
At Dr. Raza Pharma, documentation is a fundamental part of our quality management system. QA ensures that Standard Operating Procedures (SOPs), batch records, approvals, and quality documents are properly maintained to support traceability, accountability, and regulatory compliance.
The department also supports continuous improvement through quality reviews, deviation management, corrective and preventive actions (CAPA), and ongoing process evaluation.
Dr. Raza Pharma’s Quality Assurance Department represents our commitment to maintaining quality, compliance, and responsibility throughout every stage of pharmaceutical manufacturing.
Before Production
Before manufacturing begins, Quality Assurance at Dr. Raza Pharma ensures that all required materials, equipment, production areas, and documentation are properly reviewed and approved.
QA verifies that manufacturing activities begin under controlled conditions by ensuring compliance with approved procedures, readiness of facilities, and adherence to established quality standards.
During Manufacturing
During the manufacturing process, the QA team continuously monitors critical operations, process controls, documentation practices, and compliance requirements.
Through effective supervision and review, QA helps maintain consistency, prevent deviations, and ensure that every manufacturing activity is performed according to approved procedures and Good Manufacturing Practices (GMP).
Address
44-C, Industrial Estate, Hayatabad, Peshawar, Pakistan.
info@drrazapharma.com
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Phone
+92 (91) 816015 / 816125