Tipromed s.r.l. was founded in 2010 by partners with decades of experience in the biomedical field.
Its manufactured products were first sold in 2011 after obtaining EC certification for peripheral venous safety catheters with closed system , which is and always has been the Company's core business. This device was originally only sold in Italy, but its sales are now expanding both in volumes and in geographic distribution areas.
Tipromed srl's corporate policy is based on the Quality of the medical devices manufactured, with the aim of protecting the health of Patients and Health Care Workers. Such prerogative is at the base of its entire process, using only the best materials, and designing ergonomic and functional solutions allowing a safe use of the devices, even under the most unfavourable conditions of use for the Operator, and simultaneously ensuring safety and optimum comfort for the Patient.
Key factors of Tipromeds success are a skilled internal design team and technically advanced production facilities. All the staff at Tipromed s.r.l. are in close contact with the technicians monitoring project implementation, they also undergo full training that enables them to identify and immediately eliminate any defects that may arise during production. Tipromed s.r.l. considers staff training and continuous updating as fundamental elements to keep the quality of its manufactured products high.
The logistic structure of the Tipromed Ltd. plant located in the province of Reggio Emilia currently covers a total area of about 4900 m2, with 3400 m2 of covered area, and is equipped with controlled contamination environments, laboratories for Quality control, offices and warehouses. The plant was designed and built taking all the precautions necessary to prevent even the smallest changes in temperature and contamination of materials and products during storage. Tipromed s.r.l. works at its best levels to preserve the quality of its products over time.
Tipromed products' manufacturing starts with moulded or extruded components. These components are manufactured by qualified suppliers in accordance with Tipromed's specifications. The automatic and semiautomatic assembly of the particular components of each device is carried out according to a pre-defined order of processing in a class 8 controlled contamination environment according to ISO 14644. The assembly lines, mostly created internally, are equipped with on-line automatic controls establishing the correct implementation of all operations carried out. The products are packaged as always in a controlled contamination environment of the products, then sterilised by Ethylene Oxide by using a validated process according to ISO 11135. Such treatment is performed by a certified external company. In order to ensure the Quality of manufactured products, Tipromed s.r.l. strictly monitors all the steps of production that lead to each device's completion.