Quality Assurance
Quality Assurance
Quality Built into Every Process
Quality is not inspected into our products—it is built into every stage of manufacturing.
At Evans Baroque, our Quality Assurance and Quality Control systems oversee the complete product lifecycle, ensuring compliance with applicable regulatory and Good Manufacturing Practice (GMP) requirements.
Every department works together to maintain a culture of quality that prioritizes patient safety above all else.
Our Quality System
Our integrated quality management system encompasses:
- Supplier qualification
- Raw material inspection
- In-process quality monitoring
- Batch documentation
- Laboratory testing
- Product release procedures
- Change control
- Deviation management
- Corrective and preventive actions (CAPA)
- Product traceability
These systems help ensure that every product consistently meets approved quality specifications before reaching healthcare providers and patients.
Regulatory Compliance
Evans Baroque operates a pharmaceutical manufacturing facility inspected by Nigeria’s National Agency for Food and Drug Administration and Control (NAFDAC).
Our manufacturing operations follow current Good Manufacturing Practice (cGMP) principles and are designed to comply with applicable pharmaceutical regulatory requirements.
Compliance is supported through:
- Documented procedures
- Personnel training
- Internal quality reviews
- Equipment qualification
- Process validation
- Continuous monitoring
These activities reinforce our commitment to manufacturing products that meet regulatory expectations and international quality standards.
Our Quality Control Commitment
We believe quality is achieved through:
- Scientific discipline
- Continuous improvement
- Regulatory compliance
- Operational excellence
- Accountability
- Patient-focused manufacturing
Every batch released represents our promise to healthcare professionals and the communities we serve.
