Overview:
In this webinar we will focus on how to effectively manage the numerous Pressure Relief (Safety) Devices and Valves in a typical facility, and how to quickly validate them for process changes.

These devices are key safeguards to protect mechanical integrity and are sized and designed to protect piping and equipment from abnormal overpressure conditions that could result in a loss of containment. These critical overpressure devices must be maintained, and their relief capacity validated for any changes from the design process conditions. Relief device calculations are complex and can sometimes involve outside firms or contacting the manufacturer. Ensuring your process data, maintenance, MOC, and other critical documentation is accurate and accessible simplifies and streamlines the process and contributes to the accuracy of calculations and an effective Pressure Relief (Safety) Device (PRD) programme.

Key Webinar Focus / Agenda:

• Are you aware of key factors for managing the pressure relief device cycle?
• Are you maintaining and documenting your PRD service history?
• Can PRD processes and design data be readily retrieved?
• Are you adequately addressing Management of Change regarding PRDs?
• Do you have internal capabilities to verify a PRD’s capacity for process changes?
• Has the applicability for different process overpressure scenarios been considered?