Certifications

Certifications

Our commitment to quality, safety, and industry standards

At Daktari Biotechnology, we adhere to the highest industry standards and best practices. Our certifications demonstrate our commitment to quality, safety, environmental responsibility, and ethical business practices in all aspects of our operations.

Quality Certifications

ISO 9001:2015

ISO 9001:2015

Quality Management System certification demonstrating our commitment to consistent quality and customer satisfaction.

Initial Certification:2018
Next Renewal:2024
ISO 13485:2016

ISO 13485:2016

Medical Devices Quality Management System certification for our medical device development and manufacturing processes.

Initial Certification:2019
Next Renewal:2025
Good Manufacturing Practice (GMP)

Good Manufacturing Practice (GMP)

Certification ensuring our manufacturing facilities meet international standards for pharmaceutical production.

Initial Certification:2017
Next Renewal:2023
Good Laboratory Practice (GLP)

Good Laboratory Practice (GLP)

Certification for our laboratory operations, ensuring reliable and reproducible test results.

Initial Certification:2018
Next Renewal:2024
Good Clinical Practice (GCP)

Good Clinical Practice (GCP)

Certification for our clinical research activities, ensuring ethical and scientific quality standards.

Initial Certification:2020
Next Renewal:2026
Pharmacy and Poisons Board (PPB) Certification

Pharmacy and Poisons Board (PPB) Certification

Local regulatory certification for pharmaceutical manufacturing and distribution in Kenya.

Initial Certification:2016
Next Renewal:2023

Environmental & Safety Certifications

ISO 14001:2015

ISO 14001:2015

Environmental Management System certification demonstrating our commitment to minimizing environmental impact and promoting sustainability.

Initial Certification:2019
Next Renewal:2025
ISO 45001:2018

ISO 45001:2018

Occupational Health and Safety Management System certification ensuring a safe and healthy workplace for all employees.

Initial Certification:2020
Next Renewal:2026

Our Certification Process

Maintaining our certifications requires rigorous processes and continuous improvement. Our approach to certification includes:

Comprehensive Documentation

We maintain detailed documentation of all processes, procedures, and quality controls to ensure compliance with certification requirements.

Regular Internal Audits

Our quality team conducts regular internal audits to identify areas for improvement and ensure ongoing compliance with certification standards.

External Verification

Independent certification bodies conduct regular audits of our facilities and processes to verify compliance and maintain certification status.

Continuous Improvement

We implement a continuous improvement approach, regularly updating our processes and systems to meet evolving standards and best practices.