About Company
CBF Pharma Co., Ltd. is a modern and standardized company engaged in the manufacturing, processing, importing, and exporting of pharmaceuticals, medicinal materials, and chemicals.
With a commitment to participating in national socio-economic development—specifically promoting good health, accessibility, and the use of quality medicines and medical products—CBF Pharma Co., Ltd. was established under the laws of the Lao PDR and began its manufacturing and trading operations on January 1, 1995. Our objective is to develop and promote the domestic pharmaceutical manufacturing industry, advancing the supply of medicines and medical products to meet international standards.
Over the past 31 years, CBF Pharma Co., Ltd. has grown steadily from small-scale manufacturing to medium and large scale, utilizing modern technology. The CBF pharmaceutical factory operates according to Good Manufacturing Practice (GMP), features a laboratory with GLP standards, and maintains a quality management system meeting ISO 9001:2015 and ISO/IEC 17025:2017 standards. With skilled, experienced, and expert staff and workers, CBF's pharmaceutical and medical product manufacturing and business operations have advanced to a leading level in the Lao PDR.
Standard of Company
Committed to creating quality products and services to meet customer satisfaction.
Core Values
CBF is engaged in maintaining community health and taking social responsibility.
Our Vision
Committed to developing CBF into a leading manufacturer and distributor of medicines and medical equipment in the Lao PDR, integrating with the region and internationally.
Our Mission
- Manufacture and distribute medicines with international standard quality at reasonable prices.
- Provide modern medical equipment with international standards for diagnosis and treatment.
- Develop CBF to create a difference and ensure continuous growth.
Quality Policy
Committed to creating quality products and services to meet customer satisfaction.
Quality Management and Control
A journey of commitment to developing manufacturing and service excellence
GMP
Since 2003, CBF has implemented Good Manufacturing Practice (GMP), a comprehensive quality management system covering all production steps from raw materials to finished products.
GMP
By April 2004, CBF received ASEAN GMP certification for sterile injectable production from the Ministry of Health, becoming the first pharmaceutical factory in the Lao PDR to achieve this.
ISO 9001:2015
Since late 2015, CBF has applied ISO 9001:2015 quality standards to its operations to ensure high-quality, reasonably priced products, prioritizing safety from delivery all the way to the consumer.
GLP
By late 2019, the CBF pharmaceutical factory laboratory was certified for Good Laboratory Practice (GLP) according to WHO guidelines for quality control of raw materials, active ingredients, and packaging, ensuring all quality factors are controlled.
In 2023, CBF achieved the ISO/IEC 17025:2017 international standard for testing laboratory competence.