Bionap S.r.l. has been involved in a process of continuous improvement for several years in terms of management systems and product manufacturing by deploying a Science and Certification strategy. The Quality policies are intended to ensure the selection of service providers who comply with Bionap’s ethical and sustainability principles. Furthermore, the Quality policies are meant to ensure the respect of diversity across all the Company’s stakeholders. Our pursuit of Quality is reflected in our System and Product Certifications.
SOURCING
Our quality standards are applied starting from the selection of Suppliers and raw materials.
Bionap only uses raw materials from suppliers capable of satisfying our specific quality requirements. The test checks that the raw materials comply with their own specifications and are analyzed according to a self-control plan to ensure a good starting point, ensuring traceability and origin. Our network of suppliers is evaluated considering stringent requirements and approved by means of regular audits. Only an inspected supplier is considered qualified.
TESTING
Bionap operates with internal microbiology and analytical chemistry laboratories which include highly qualified staff and cutting-edge equipment. Our facilities perform a wide range of rigorous controls. Tests on raw materials, intermediate and finished products include microbiological analysis and chemical determinations of active compounds and contaminants. All this follows the Good Laboratory Practices, essential for quality control. Furthermore, it collaborates with some external laboratories recognized and certified by bodies such as Accredia and the Ministry of Health.
FACILITY AND PRODUCTION
Our facilities and standard procedures adhere to the stringent regulations of Good Manufacturing Practices and HACCP (dietary supplements). Operating in compliance with GMP, we follow the entire production chain, starting from raw materials, to semi-finished products and up to finished products. Our manufacturing team undergoes training to ensure consistent adherence to protocols for quality, hygiene, and documentation.
The release of the batches derives from the positive results obtained from the timely analyses performed on each production batch: organoleptic parameters, active compounds, contaminants and microbiology. After the batch release, a sample of each authorized batch is retained for post-release controls, including stability studies. The main basic requirement is to comply with the laws and regulations, taking also in consideration where the product is marketed.
Corporate Certifications
Product Certifications
