Jeloga proposes benefits study, advice and integration for the definition, design and validation of instrumented functions of security (IFS), according to standards of functional security IEC 61508, 61511, 13849, 62061.
Study, advise and integrate your machines in complete safety
The requirements with which the company is confronted grow from day to day. The evolutions of the standards, the constant improvement of productivity can be risks factors for the company. Jeloga Engineering helps to minimize these risks, by respecting the specific needs of the customer :
Jeloga Engineering offers a LCCM system (Life Cycle Cost Management), which is a co-operation with the customer with the aim of an optimization of the systems of production in the long-term (preventative maintenances, inspections, updates, put into the standards of installations and more).
The validation of a pharmaceutical and biotechnological production installation is a requirement of the FDA (Food and Drug Administration). To authenticate and qualify an installation, the sector of the process automation follows rules elaborated according to the GAMP (Good Automated Manufacturing Practice). Jeloga Engineering optimized its working processes to assure a minimized cost, an appropriate instruction and a qualification of equipments according to the requirements of the FDA.
- Analyses of risks HAZOP, HAZID, AMDEC
- Definition of the instrumented functions of security and levels SIL required
- Graphs of calibrated risks
- Matrix of safety barriers
- Definition of the architectures of automatisms
- Calculation of reliability and availability (PFD, PFH & SFF)
- Analysis of the measures of prevention and reduction of the risk
- Engineering of protectors, control devices and electric, mecanic, hydraulic, pneumatic risk reduction devices
- Procedures of maintenance and inspection
Jeloga Engineering offers a LCCM system (Life Cycle Cost Management), which is a co-operation with the customer with the aim of an optimization of the systems of production in the long-term (preventative maintenances, inspections, updates, put into the standards of installations and more).
The validation of a pharmaceutical and biotechnological production installation is a requirement of the FDA (Food and Drug Administration). To authenticate and qualify an installation, the sector of the process automation follows rules elaborated according to the GAMP (Good Automated Manufacturing Practice). Jeloga Engineering optimized its working processes to assure a minimized cost, an appropriate instruction and a qualification of equipments according to the requirements of the FDA.