Regulatory
Manufacturers of medical devices based outside the EU must designate an Authorized Representative (EC-REP) established within the EU in order to meet the CE requirements for placing medical devices on the EU market.
Quality Management
Regen Lab Quality System Management ensures the consistency of our products quality in total GMP compliance.
Our production facility rooms atmosphere is monitored to satisfy non-pyrogenic medical devices manufacturing.
Patents
As a leader in the PRP&HA regenerative field and as an innovation-driven company, Regen Lab SA has devoted important resources since 2004 to put on the market pioneering and diversified products constituting a complete set of tools/technologies for the medical community.