The Sustainable Food & Drug certification confirms that a food product, dietary supplement, pharmaceutical or medical product is produced and managed in a responsible environmental, organizational and social manner, taking into account the entire value chain.
In the food and pharmaceutical sectors, trust is fundamental. Safety, quality, traceability and regulatory compliance are not optional — they define market credibility. LIBRE certification is not a marketing label. It is a verification process based on audit, measurable criteria and documented evidence.
The LIBRE EIS system evaluates:
Certification applies not only to the product itself, but also to production processes, storage, distribution and organizational governance.
During the certification process, the producer is required to:
The producer bears full responsibility for the accuracy of disclosed information.
The certification is based on a structured assessment of key areas:
???? Energy
Share of renewable and alternative energy sources in total energy consumption.
???? Water Management
Responsible water management, including reuse, retention and treatment systems.
???? Human Factor
Workforce management, safety standards, CSR engagement and operational organization.
???? Bio Production
Verification of biological production standards where applicable.
Final results are expressed in a performance class (A+–E) based on measurable criteria.
The certification is dedicated to:
Audits are conducted by certified LIBRE professionals (International Energy Efficiency Auditor), and in the case of new facilities also by International Energy Efficiency Designer.
Bio Production verification may be conducted directly by LIBRE Foundation.
The certification:
The food and pharmaceutical industries face increasing regulatory, investor and consumer pressure.
Sustainable Food & Drug certification:
This is not a declaration of sustainability.
It is a verified management system.