The sale of its products is carried out by its three specialized divisions: the Pharmaceutical Technology Division, the Laboratory Equipment Division and the Industrial Vacuum Division.

Telstar products and systems rely on technical features which are carefully thought-out in order to facilitate operations in accordance with guidelines and regulations pertaining to each particular industry; health and safety, intrinsic quality, etc. For example, in the case of equipment for pharmaceutical laboratories, the GxP regulations (GLP, GCP and GMP), the FDA's (21 CFR) recommendations, the GAMP correct automation regulations, the European Union regulations (EN regulations), etc. are all taken into account. In addition to the CE label, our quality assurance policy demands that certain products receive quality certification such as the TـV Cert. or ETL, among others.

Telstar follows design and production practices in accordance with the ISO 9001 international quality standard. For example, with customised installations, design qualifications (DQ), installation qualifications (IQ1 and IQ2) and exhaustive tests and documentation are all normal practice at Telstar. Our objective is to provide a final product which we are totally satisfied with.

For more information refer to site www.etelstar.com