Quality Assurance

 

At Pearl Pharmaceuticals, our Quality Assurance (QA) Department plays a crucial role in ensuring that every product meets the highest standards of safety, efficacy and compliance. Our commitment to quality and excellence is at the core of our operations, ensuring that we deliver trusted and effective pharmaceutical solutions to our customers.

Key Responsibilities of the QA Department:

 

1. Regulatory Compliance:

   • Ensuring adherence to cGMP (current Good Manufacturing Practices), WHO guidelines, and other international quality standards.
   • Conducting regular audits and inspections to maintain compliance with regulatory bodies.

2. Quality Control & Testing:

   • Monitoring and evaluating raw materials, in-process production, and finished products.
   • Conducting stability studies, microbiological testing, and analytical testing to maintain product integrity.

3. Process Validation & Documentation:

   • Implementing stringent SOPs (Standard Operating Procedures) for production and quality control.
   • Maintaining detailed batch records, deviation reports, and risk assessments to ensure traceability.

4. Continuous Improvement & Training:

   • Identifying areas for process enhancement and quality improvement.
   • Conducting regular training sessions for employees to uphold best practices in pharmaceutical manufacturing.

5. Customer & Market Feedback Analysis:

   • Monitoring customer complaints and market feedback to ensure continuous product enhancement.
   • Implementing corrective and preventive actions (CAPA) for consistent product quality.

At Pearl Pharmaceuticals, our QA team is dedicated to ensuring that every medicine we produce is safe, effective, and of the highest quality, reinforcing our mission of delivering healthcare solutions you can trust.