4000+
Square-metre purpose-built facility
Future-Ready Pharmaceutical Manufacturing
Manufacturing Built Around Quality, Control, and Responsible Growth
Pharma One brings specialized production lines, dedicated manufacturing sections, laboratory support, organized packaging, integrated safety, and partner-ready capability together in one purpose-built pharmaceutical facility in Kabul.
16
Specialized production lines
3
Dedicated production sections
2018
Manufacturing company established
Manufacturing Overview
A Purpose-Built Facility for Coordinated Pharmaceutical Operations
The Pharma One facility brings production, laboratory, packaging, warehousing, utilities, administration, conference, and training functions into one organized environment. Its layout supports controlled movement, operational coordination, documentation, and a practical foundation for future expansion.
Juma Mohammad Mohammdi, Industrial Estate 2nd Phase, Nasaji Bagrami, Kabul Afghansitan
Pharma One · Kabul Medicine Factory
Modern infrastructure, disciplined systems, laboratory support, and expansion-ready planning.
Three Dedicated Production Sections
Separated Manufacturing Capability Across Key Dosage Forms
Dedicated production sections support clearer control, organized movement, specialized handling, and focused quality attention across the facility.
General Medicines Section
A flexible multi-dosage manufacturing area supporting commonly used pharmaceutical forms through organized production, in-process control, and coordinated packaging.
- Liquid Syrup
- Dry Suspension
- Tablets
- Capsules
- Sachets
- Creams
- Lotions
Penicillin Section
A dedicated area designed for penicillin products with separated handling, controlled movement, documented processes, and focused quality oversight.
- Dry Suspension
- Tablets
- Capsules
Cephalosporin Section
A specialized production section supporting cephalosporin dosage forms through dedicated workflows, controlled environments, and quality-focused manufacturing practices.
- Injections
- Dry Suspension
- Capsules
Integrated Capability
From Manufacturing to Product Readiness
Production, testing, documentation, packaging, partner coordination, and development support work together as one connected manufacturing system.
Medicine Production
Organized pharmaceutical manufacturing across multiple dosage forms, supported by documented procedures, trained teams, and coordinated production planning.
In-Process Quality Control
Checks during manufacturing support batch consistency, process discipline, documentation accuracy, and timely identification of deviations.
Laboratory Testing
Chemical, microbiological, sterility, stability, raw-material, in-process, and finished-product testing capabilities support quality decisions.
Packaging & Labeling
Coordinated packaging and labeling improve product identity, batch clarity, handling control, presentation, and readiness for distribution.
Partner Manufacturing
Third-party manufacturing can support agreed formulations, specifications, packaging requirements, quality checks, and documented partner coordination.
Product Development Support
Formulation work, stability planning, documentation, laboratory review, packaging coordination, and scale-up preparation support future product development.
Controlled Production Flow
A Clear Path From Materials to Finished Product
Every major stage is supported by defined responsibilities, documented records, controlled handling, quality review, and coordinated handover.
01
Material Receipt & Review
Raw and packaging materials are received, identified, documented, and directed through the required review and storage process.
02
Production Planning
Approved requirements are translated into organized batch planning, line preparation, material coordination, and documented responsibilities.
03
Controlled Manufacturing
Manufacturing activities follow defined steps with attention to environment, equipment readiness, operator practices, safety, and process records.
04
Testing & Batch Review
In-process checks and laboratory results are reviewed with production records to support documented quality decisions.
05
Packaging, Release & Handover
Approved products move through packaging, labeling, final review, controlled storage, and coordinated handover for distribution.
Manufacturing Infrastructure
Designed Around Control, Safety, Coordination, and Growth
Infrastructure and utilities are organized to support suitable pharmaceutical working environments, safe operations, coordinated movement, and future manufacturing expansion.
Controlled Air Systems
HVAC, fresh-air support, air-lock access, and controlled movement help maintain suitable pharmaceutical working environments.
Integrated Safety
Fire detection, emergency access, surveillance, utility planning, and operational controls are integrated across the facility.
Organized Production Flow
Production, laboratory, packaging, storage, utility, and administrative functions are arranged to support controlled daily coordination.
Expansion-Ready Design
Purpose-planned spaces and utilities provide a practical foundation for additional capability, equipment, and future manufacturing growth.
Your Brand, Our Manufacturing Precision
Build Your Pharmaceutical Product With Pharma One
Discuss product development, third-party manufacturing, packaging, quality-control support, and local production opportunities with the Pharma One team. Every project remains subject to technical review, required approvals, and agreed specifications.