Phil is Senior Test and Validation Engineer at PRISYM ID, assisting our clients in meeting regulatory compliance to FDA, MHRA, EU and GMP for the company software products supplied to the life sciences industry. He also ensures that validation documents and processes are in line with current regulatory guidance, and delivers onsite training for PRISYM ID’s proprietary software. He provides test plans and processes to ensure software products are robust before release.

What do you hope the audience will learn from this webinar?

The importance of leveraging supplier documents and personnel to potentially reduce your validation effort by using a structured and defendable approach.

What discussions do you look forward to having with the audience?

Discussions about the process to achieve a leveraged position and the content of supporting documents what can be effectively used.

What do you enjoy most about your role?

Assisting in finding the least burdensome approach to validation whilst assisting clients in maintaining and observing their regulatory obligations.

How did you get into the industry?

It seemed to be a natural progression from a software testing role which then combined with Validation activities to result in a Test and Validation role.

Where is your favourite place in the world and why?

I don’t really have a favourite place in the world, just anywhere which offers relaxation and where I can get away from mobile communications.

Join Phil in the PRISYM ID webinar “Mind the Gap! Labeling Experts share the 7 Steps of building a Global Labeling System and reducing the Validation effort“