PHARMA, BIOTECH &

HEALTHCARE

Organizations, which are active in the domain of Pharma – Biotech – Healthcare, are all required to implement a compliant and consistent risk-based Quality System. The prevention and the rational estimation of the risk of contamination is always a strong requirement of the applicable GMP regulation. In Kernelis, we do have an extensive expertise and experience with these regulatory systems.

The technology gives the means to rationally demonstrate the control and the compliance of the Organization for the following topics: Risk Management, Knowledge Management, Quality System, Data Integrity, Prevention of Cross-Contamination, Risk Exposure, Cleaning Validation, Design and Qualification of production Infrastructure, premises and equipment.

Since the computerized systems of Kernelis were designed to be fully validated in compliance with GMP requirements, this technology will provide the Client with the highly valued merit of being accepted by Competent Bodies.

CRUCIAL

MODULES

Resilience

Risk, Resilience & Reinforcement

Kernelis Resilience is by design perfectly adapted to control Risk and Resilience issues in the sector of GMP regulated activities. The Software has already been presented and even reviewed during formal inspections by Competent Bodies of Kernelis Client. To demo the performance of the Software in this domain, Kernelis has developed a specific case study which can be watched upon request.

Exchange

Exposure Risk Assessment,

Thermal Balance Evaluation

Meshing

Automated Scan-to-CAD

Processing

Propagation

Explosion & Propagation

Modeling

Kernelis Exchange, Meshing & Propagation should be used to combine their specificities to assess the performance of the infrastructure. Potential situation of cross-contamination, with the rational determination of the Permitted Daily Exposure and the OEL/STEL values for operators, can thus be assessed.