Good Manufacturing Practices (GMP) for Kenyan Pharmacies

by Mr. Maroa Noa | Nov 19, 2025 | Legal Framework, Operations, Risk Management, Strategy

What is GMP and Why Does It Matter?

Good Manufacturing Practices (GMP) are internationally recognized principles that ensure pharmaceutical products are consistently produced and controlled according to quality standards.

In Kenya, GMP regulations are enforced by the Pharmacy and Poisons Board (PPB) to guarantee the safety, efficacy, and quality of medicines distributed across the country.

For both pharmaceutical manufacturers and community-level dispensaries, adhering to GMP guidelines is not optional—it’s a fundamental obligation.

In this article, we’ll explore Kenya’s GMP framework, compliance requirements, and practical strategies to maintain GMP standards across pharmaceutical operations.

Understanding the GMP Regulatory Framework in Kenya

GMP in Kenya is regulated under the Pharmacy and Poisons Act (Cap 244) and various PPB-issued guidelines.

The PPB, in collaboration with international agencies like the WHO, has adopted and localized GMP standards to suit the Kenyan pharmaceutical context. These standards apply to:

• Drug manufacturers
  
• Importers and exporters
  
• Warehouses and distributors
  
• Contract manufacturing and packaging facilities

GMP inspections are routinely conducted to assess compliance, and failure to meet the requirements can lead to suspension of operations or product recalls.

Key Pillars of Good Manufacturing Practices

1. Quality Management Systems (QMS)

A quality management system (QMS) is a structured framework that defines and documents an organization’s processes, procedures, and responsibilities for achieving quality policies, practices, and objectives.

The goal of a QMS is to reduce waste, increase efficiency, and improve customer satisfaction. A strong QMS is the backbone of GMP compliance. It includes:

2. Personnel and Training

Every employee involved in manufacturing must be:

• Trained on GMP requirements
  
• Competent in their specific tasks
  
• Regularly evaluated for performance and knowledge

The PPB emphasizes that all staff should understand hygiene practices, documentation standards, and contamination prevention techniques.

3. Premises and Equipment

Facilities must be constructed to minimize contamination. Requirements include:

• Smooth, easy-to-clean surfaces
  
• Controlled airflow and temperature
  
• Segregated zones for different processes
  
• Validated and calibrated equipment

This ensures that both raw materials and finished products are protected from physical, chemical, or microbial hazards.

4. Documentation and Record-Keeping

“If it’s not documented, it didn’t happen”—this GMP mantra highlights the importance of good record-keeping. Essential documents include:

• Batch manufacturing records
  
• Equipment logs
  
• Cleaning schedules
  
• Deviation reports
  
• Stability testing data

Digital documentation systems are increasingly being adopted in Kenya for enhanced traceability and data integrity.

5. Raw Material Control

All raw materials must be:

• Sourced from approved suppliers
  
• Tested for identity, purity, and quality
  
• Properly labeled and stored

The PPB requires full traceability for every input used in the manufacturing process.

Common GMP Violations in Kenyan Pharmacies and Manufacturers

Non-compliance with GMP can lead to serious consequences. Common violations observed by the PPB include:

• Inadequate or missing documentation
  
• Cross-contamination due to poor layout
  
• Untrained staff handling sensitive tasks
  
• Failure to conduct quality testing on finished products
  
• Expired materials used in manufacturing

These lapses not only risk public health but also damage brand reputation and can lead to legal action or operational suspension.

GMP Inspection and Certification Process in Kenya

Here is how the process typically works in Kenya:

Step 1: Preparation and Application

The manufacturer completes the application form (via the PPB online portal) and submits required documents.
After submission, PPB issues an invoice and payment must be settled.

Step 2: Scheduling the Inspection

Once documentation is in order, PPB arranges a site inspection. The inspection covers manufacturing premises, equipment, processes, personnel competence, documentation, quality control and more.

Step 3: On-site Inspection

Inspectors evaluate the site against criteria in the GMP guidelines: site design and cleanliness, process controls, documentation, product quality systems, storage, personnel training, etc.

If there are discrepancies, inspectors raise observations and may require corrective actions (CAPAs).

Step 4: Report and Corrective Actions

After the inspection, PPB issues an inspection report, highlighting non-compliance issues if any. The manufacturer must respond with corrective actions and implement them within a set timeframe.

Step 5: Certification / Approval

If the manufacturer meets the GMP requirements and resolves any major issues, PPB issues a GMP certificate or approval.

The certificate may be required for regulatory approvals, export permissions, etc.

Step 6: Ongoing Compliance & Surveillance

GMP certification is not a one-off event. PPB conducts surveillance inspections periodically to ensure continued compliance. Manufacturers must maintain standards, update SOPs, train staff and audit internal systems.

Benefits of GMP Compliance for Kenyan Pharmaceutical Businesses

Complying with GMP brings a host of advantages, including:

• Regulatory Approval: Facilitates PPB licensing, registration, and product marketing
  
• Market Trust: Builds consumer and healthcare provider confidence
  
• Reduced Recalls: Minimizes the risk of product failure or public health hazards
  
• Operational Efficiency: Standardized procedures lead to fewer errors and better outcomes
  
• Global Opportunities: GMP certification opens the door to regional and international markets

Digital Transformation in GMP Compliance

The PPB is encouraging the adoption of digital tools to improve GMP compliance. Key innovations include:

• Electronic Batch Records (EBR): Reduce errors and improve audit readiness
  
• Digital Quality Management Systems: For real-time tracking of SOPs and deviations
  
• Mobile Training Modules: To ensure staff are consistently educated on best practices
  
• Environmental Monitoring Systems: Automated systems to monitor temperature, humidity, and air quality in real-time

Digital solutions not only streamline compliance but also offer cost savings and scalability for growing pharmaceutical businesses.

Challenges to GMP Compliance in Kenya

Despite clear guidelines, some facilities struggle due to:

• High costs of facility upgrades
  
• Limited access to trained GMP consultants
  
• Resistance to documentation and SOP adherence
  
• Inconsistent enforcement across counties

To address these challenges, the PPB collaborates with training institutions and donor partners to offer workshops, audits, and financial support to manufacturers.

A Foundation for Safe and Quality Medicines

Good Manufacturing Practices are the cornerstone of pharmaceutical safety and quality assurance.

In Kenya, adherence to GMP ensures that patients receive safe, effective, and high-quality medicines, while pharmaceutical businesses maintain compliance, credibility, and competitiveness.

With increasing regulatory oversight and digital innovation, Kenyan pharmacies and manufacturers are better equipped than ever to implement GMP successfully.

By investing in quality systems, training, and facility upgrades, every stakeholder in the pharmaceutical supply chain can contribute to a healthier, more trustworthy healthcare system.

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