Production, QHSES & Compliance

HSE Remediation Plan

Project

As part of a project to remediate HSE actions on a pharmaceutical production site, implementation of actions and monitoring indicators for the various HSE processes.

Documentary actions to update procedures and field actions such as implementation of the LOTO methodology, deployment of URS HSE on the site.

Duration Project

8

months

Production site

Dry form

Expertise

Challenges

Services provided

Computerised System Validation

Quality management system for medical devices, the ISO 13 485 standard and the impact of the new RDM 2017/745 regulation​