
Quality Management
Our comprehensive approach to ensuring excellence in all we do
At Daktari Biotechnology, quality is at the core of everything we do. Our comprehensive Quality Management System ensures that our products, services, and processes consistently meet the highest standards of safety, efficacy, and reliability.
Our Quality Policy
Daktari Biotechnology is committed to developing and manufacturing high-quality biotechnology products that meet or exceed customer expectations and comply with all applicable regulatory requirements. We achieve this through:
Implementing and maintaining an effective Quality Management System that complies with international standards
Ensuring all employees understand their role in maintaining quality and are properly trained
Continuously monitoring and improving our processes, products, and services
Fostering a culture of quality awareness and responsibility throughout the organization
Establishing quality objectives and regularly reviewing performance against these objectives
Providing the necessary resources to maintain and improve our Quality Management System
"Quality is not just a department at Daktari Biotechnology—it's a responsibility shared by every member of our team."
— Dr. James Mwangi, Chief Executive Officer

Quality Management System
Quality Control
Our rigorous testing protocols ensure that all products meet specified requirements before release.
Quality Assurance
We implement systematic activities to ensure that quality requirements will be fulfilled.
Documentation Control
Comprehensive documentation systems ensure traceability and compliance with regulatory requirements.
Performance Monitoring
Regular monitoring and analysis of key performance indicators to drive continuous improvement.
Training & Development
Ongoing training ensures all staff have the knowledge and skills to maintain quality standards.
Supplier Management
Careful selection and monitoring of suppliers to ensure quality throughout our supply chain.
Our Quality Certifications

ISO 9001:2015

ISO 13485:2016

GMP Certified

GLP Certified
Continuous Improvement Process
Plan
Establish objectives and processes necessary to deliver results in accordance with specifications.
Do
Implement the processes and collect data for analysis in the following steps.
Check
Study the actual results and compare against the expected results to identify any differences.
Act
Take actions to improve performance, as necessary. Analyze the differences to determine their cause.