Pharmaceutical industry: zero tolerance, total traceability
Pharmaceutical and over-the-counter drug manufacturing and storage facilities operate under the supervision of the Federal Agency for Medicines and Health Products (AFMPS) and, for facilities exporting to the United States, the FDA. In these environments, the presence of even a single pest can compromise an entire production batch and trigger a recall.
L'approche EGN Expert pour l'environnement pharmaceutique :
Fiabilité
Procedures compatible with the requirements of controlled environment areas (clean rooms, controlled atmosphere zones): adapted products and methods, with no risk of cross-contamination.
Reporting
Complete and timestamped documentation of each intervention, directly usable in your GMP compliance file.
Compétences
Continuous training of our technicians on the specific requirements of the pharmaceutical sector, beyond the common baseline required by the CEPA EN 16636 standard.
Traçabilité
Digital client portal allowing your quality assurance manager to consult, at any time, the complete history of interventions and trend analysis by area.
GMP
Reach new heights.
Environment
Reasoned fight - Controlled environmental impact.
A CEPA Certified partner
A guarantee of trust for your auditors
Focus on the
quality and reporting
Online reporting, trend analysis 24/7
Our CEO: over 14 years of experience in the pharmaceutical sector
Join us and shift into high gear.