Laboratoire POLIDIS has an internal regulatory affairs department, ensuring perfect mastery of the regulations in force.
Laboratoire POLIDIS ensures complete traceability of all its products, from manufacture to delivery to its customers.
CONTROLLED MANUFACTURING
CERTIFIED QUALITY
The ongoing strife for customer satisfaction is the main driving force behind the Laboratoire POLIDIS approach to quality.
The LNE/G-MED, a notified certifying body whose demands are recognised internationally, carries out annual inspection and auditing of the Laboratoire POLIDIS quality management system.
According to Laboratoire POLIDIS, conceiving and developing medical devices that correspond to international quality standards means:
Complying with the ISO 13485 standard
Meet CE requirements and regulatory changes
Satisfying customers
Laboratory POLIDIS’s Quality Policy relies on the following items :
- maintain a quality management system complying with the regulatory requirements of the CE mark, Public Health Code and the principles of NF EN ISO 13 485: 2016
- Provide ongoing responsiveness to customers requirements
- Involve staff in a constant process of improving the products and services quality over time
