BPI recruits highly competent management and personnel, uses state-of -the art facilities and complies with international standards to ensure that each product is top quality.
We pride ourselves on having earned a number of International, regional, and local certificates.
BPI has acquired the Good Manufacturing Practice (GMP), ISO 9001: 2015 Quality Management System, and our medical devices meet the high standards of the European Union and they have acquired the ISO 13485:2016 Medical devices -Quality management systems- Requirements for regulatory purposes as well as the CE marking.
BPI has two multipurpose industrial operations sites for the manufacturing of pharmaceutical and medical devices, in Dbayeh, Lebanon, and in Lyon, France.
Future plans include new manufacturing facilities in Europe, the Middle East, and Africa.
Pharmaceutical Production Capabilities & GMP Compliance
The production of our pharmaceutical products is segregated into four independent units: a Conventional Pharmaceutical Production Unit, a Biological and Biotech Production Unit, a Cytotoxic Production Unit and an Antibiotic Production Unit.
Industrial operations sites and their supporting utility systems are designed to comply with the requirement of the current GMP standards in order to provide a continuous and efficient unidirectional flow of material and personnel.
The plant is designed to ensure the consistency of operations through the superior quality of equipment and utilities. It was also built to guarantee the supreme quality of products through testing at higtech laboratories for physical, chemical, and microbiological analyses.