Quality Control Department
Where Precision Defines Trust
Rasco Pharma’s Quality Control (QC) Department stands at the core of our commitment to deliver safe, effective, and reliable medicines.
Spanning over 12 000 square feet, it is Pakistan’s largest and most advanced QC laboratory, officially accredited by PNAC under ISO/IEC 17025.
Every analysis performed here reflects our belief that quality is not a stage in production , it is a continuous discipline.
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Microbiological Excellence
A dedicated Microbiology Laboratory operates independently within the QC unit, designed with controlled air classification and separate material and personnel flows.
Capabilities include:
- Sterility testing (SCF and membrane filtration)
- Environmental monitoring of classified areas
- Microbial limit and water testing
- Bioburden and Endotoxin testing
- Validation of disinfectants and cleaning processes
Research & Development Support
Our R&D laboratories for tablets, capsules, syrups, injectables and topicals operate adjacent to the QC area, ensuring rapid analytical method development and technology transfer.
The R&D team partners with formulation scientists to develop new molecules and optimize existing ones for bio-equivalence and regulatory submissions.
Compliance & Data Integrity
Every result generated is captured through 21 CFR Part 11-compliant software, ensuring traceability, audit trails and data security.
The QC Department follows Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) under the supervision of qualified analysts, chemists and microbiologists.
Through discipline, training, and technology, our Quality Control team ensures that every Rasco Pharma product delivered to the market meets international standards of purity, potency and performance.
Quality Assurance Department
Quality by Design — The Core of Our System
At Rasco Pharma, Quality Assurance (QA) is not a final check — it is the governing philosophy of our entire organization.
Our QA team oversees and controls every aspect of manufacturing and testing to ensure that our medicines consistently meet the highest standards of safety, efficacy and compliance.
Comprehensive Quality Management System (QMS)
The QA Department has implemented an integrated QMS that aligns with:
- ISO 9001 (Quality Management)
- ISO 14001 (Environmental Management)
- ISO 45001 (Occupational Health & Safety)
- ISO/IEC 17025 (PNAC Accreditation)
- PIC/S and WHO GMP Guidelines
Our QMS ensures traceability from raw material procurement to product release, supported by documented SOPs, risk management protocols and internal audits.
Core Functions of QA
- Vendor Qualification & Raw Material Approval: Ensuring only approved suppliers meet our stringent quality criteria.
- Batch Manufacturing Record Review: Thorough documentation and cross-verification before any product is released.
- Process Validation & Equipment Qualification: Comprehensive IQ/OQ/PQ to ensure reproducibility and compliance.
- Change Control & Deviation Management: Structured systems for risk evaluation and corrective actions.
- Internal Audits & Training: Regular QA-led audits and GMP training to foster a culture of quality ownership.
- Product Quality Review (PQR): Annual evaluation of every product to ensure continued efficacy and consistency.
- Document Control & Archiving: Centralized electronic system ensuring real-time updates and version control.
- Pharmacovigilance & Complaint Handling: Post-marketing surveillance and rapid response mechanisms for customer feedback.
Training & Culture
Our QA Department drives continuous education for every employee — from production staff to senior management — through regular GMP and data-integrity sessions.
The goal is to transform quality from a procedure into a shared belief system embedded in daily operations.
Digital QA Environment
Rasco Pharma operates in a paperless, software-integrated environment where batch records, deviation logs and audit reports are maintained electronically for traceability and regulatory readiness.
This digital ecosystem supports real-time decision making and facilitates cross-functional coordination between QA, QC and Production teams.
Commitment to Global Compliance
Our QA strategy is aligned with the company’s goal to achieve PIC/S certification and WHO prequalification.
We actively engage with international consultants to continuously benchmark our systems against the best in the world.
Together, our Quality Control and Quality Assurance departments form the heart of Rasco Pharma’s promise:
“To manufacture every product with the same care and precision as if it were for our own family.”
OUR PEOPLE & CULTURE
At Rasco Pharma, our greatest strength is our people.
We’ve built a workplace culture that promotes learning, collaboration, and wellbeing — enabling our teams to perform at their best.
We’ve established a modern recreational and wellness area within our facility — complete with ping-pong, pool, PlayStation, and comfortable lounge spaces — ensuring our technical and non-technical staff have opportunities to relax, recharge, and stay mentally sharp.
Our continuous training programs, leadership development initiatives, and cross-department learning modules ensure our workforce remains globally competitive and future-ready.