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Establishing a Quality Management System in Life Sciences (2026): Scope, documentation, and core processes to implement first

About this event

A 30-minute webinar for life science companies establishing a Quality Management System (QMS)

Implementing a Quality Management System (QMS) is essential for aligning business objectives with regulatory requirements, improving internal efficiency, and ensuring consistent control of quality-related activities. 

To establish a QMS, an organization must define its quality objectives, develop documented processes and procedures aligned with applicable requirements, assign roles and responsibilities, and implement mechanisms for monitoring, compliance, and continuous improvement. 

Organizations establishing a QMS could encounter avoidable implementation challenges caused by: 

-unclear definition of QMS scope, 

-poorly structured QMS documentation,

-or attempting to implement multiple core quality processes simultaneously without a defined sequence. 

We will focus on the core elements of a QMS - document management, training management, and change control - within the context of a complete QMS that includes additional quality processes not covered in this session. 

The session specifically addresses: 

-defining the initial scope of a QMS, 

-developing a structured QMS documentation hierarchy, and 

-understanding a typical use case from QMS Implementation 

This webinar is intended for organizations establishing or formalizing an early-stage QMS in 2026. 

Hosted by

  • Team member
    T
    Thomas Tschirhart Director of Sales @ SimplerQMS

    I work closely with life science companies to help them structure and scale their Quality Management Systems. With 10 years of experience in the eQMS space, I believe in bringing expertise to the front of every discussion with a focus on time to value and return on investment.

SimplerQMS

SimplerQMS provides cloud-based quality management software specifically designed for Life Science organizations, enabling them to efficiently manage regulatory documentation and automate processes through a fully validated system that includes modules...