Audits

The operating procedures at Future Diagnostics are monitored by internal and external audits. Every audit leads to corrective and preventive actions (CAPA), which result in a continuous improvement of the Quality Management System.
 

Internal Audits

Future Diagnostics has established a system for Internal Audits. All processes that affect the Quality Management System are audited at least once a year. The internal audits are conducted to determine whether the processes comply with ISO 9001, ISO 13485 and FDA Quality System Regulations and to determine whether the processes are effective and in line with the company’s policy.
 

Client Audits

The operating processes and quality system at Future Diagnostics are frequently audited by our customers. These client audits are an important aid in our continuing effort to improve our procedures and to better meet the customer's requirements.
 

Third Party Audits

Future Diagnostics accredited certification body is Lloyd’s Register Quality Assurance (LRQA). LRQA visits the company every 6 months for evaluation of the Quality Management System based on ISO 9001 and ISO 13485.

In addition, the United States Food and Drug Administration (FDA) regularly inspects Future Diagnostics for compliance with its Quality System Requirements.