EXPERTS IN PROCESS Technology
PROCESS EQUIPMENT FOR SOLIDS
EXPERTS IN PROCESS technology
PROCESS EQUIPMENT FOR SOLIDS
The employees and the value they bring are the most important in our company, this is what makes us different. Thanks to this, we are able to bring the best of ourselves to our customers, as well as the employees contribute among themselves to have a richer job and encourage the development of the human team.
Our goal is always to maintain a long-term relationship with employees, applying internal promotion policies to ensure their personal and professional development.
Our company values are aimed at forming teams in their different specialties to assist the client during all phases of the project. We are totally committed to quality: from the choice of equipment and the most appropriate solutions, to start-up and after-sales service.
OUR COMPANY MISSION
Offer innovative solutions oriented to the future needs of the pharmaceutical and related sector.
Work on our values day by day to attract and retain professional talent, only to obtain good results.
Values: Our values are based on Integrity, Commitment, Appreciation, Confidence, Passion and honest and open Communications.
- Commitment and rigor with our employees, customers and suppliers.
- Respect for the environment.
- Ethical code in the framework of our CSR (Corporate Social Responsibility)
- We reinvest more than 80% of the profits in our company.
- Involved in continuous improvement within our Quality system.
- We contribute in solidarity plans permanently.
STE PROCESS TECHNOLOGY
The design of all our equipment follows the criteria of EHEDG hygienic design code. By hygienic design we mean the application of design techniques for equipment and installations that allow the timely and effective cleaning of all machinery. The hygienic design approach incorporates preventive characteristics to these elements, those characteristics reduce or eliminate the risks of contamination. Considering aspects such as construction materials, contact surfaces, porousness, airtightness, accessibility of industrial equipment and facilities, GMP standards and the use of materials authorised by the FDA.
QUALIFICATION OF EQUIPMENT
As required by the GMP and the FDA, and in accordance with the VMP of our customers, all our equipment is qualified to guarantee the complete process control.
• Design Qualification (DQ)
• Installation Qualification (IQ)
• Operational Qualification (OQ)
• Performance Qualification (PQ)
By following these protocols STE fulfills the client’s requirements, and offers a post-installation implementation service to comply with IQ / OQ protocols.
DESIGN CALCULATION: PRESSURE EQUIPMENT
Process equipment considered to be pressure equipment is manufactured in compliance with the design code EN 12445: 2015.
• Reactors with heated sleeves
For internal security, calculations to check mechanical integrity of shock resistance, fluid beds and fittings suitable for vacuum loading, according to the EN 13445 standards are made.
COMMERCIAL ELEMENTS RULES
The commercial elements that we incorporate into our equipment are required to follow the ASME Bioprocessing Equipment (BPE) Certification Program (elements such as clamps and pipes of ASME dimensions) and the European standard EN or DIN (for main pipes and flanges).