Our Commitment
TJL Pharmaceutical exists to make world-class healthcare accessible. Every LifeSol® product leaving our Kabul facility must be safe, effective and consistent — because behind every bottle is a hospital ward, a pharmacist's shelf and a patient's recovery.
GMP Compliance
Our manufacturing operates under current Good Manufacturing Practice (cGMP) principles aligned with WHO guidance for sterile pharmaceutical preparations — covering classified cleanrooms, validated equipment, controlled environments and complete batch documentation.
Quality Management System
- Documented procedures for every production and testing stage
- Deviation, CAPA and change-control management
- Regular internal audits and management review
- Supplier qualification and incoming material verification
- Continuous training for production and laboratory staff
Quality Assurance & Quality Control
Quality Assurance oversees the entire system, while our in-house Quality Control laboratories test every batch for sterility, pyrogens, particulates and chemical specification before release. No batch reaches the market without full QC release.
Patient Safety & Traceability
Every bottle carries a batch number providing complete traceability from raw material to point of dispatch. In the unlikely event of a quality concern, batch-level traceability enables rapid, targeted action — see our Returns & Product Recall Policy.
Continuous Improvement
We measure, review and improve our processes continuously — investing in automation, laboratory capability and staff development so that quality rises with every batch produced.
Questions about this policy?
Our team responds to all policy and compliance enquiries within one business day.
contact@tjlhealthcare.com