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Autorenbild Max Meidl

Max Meidl

Head of Quality and Compliance Management
Max Meidl stands for safety and quality. As Head of Quality and Compliance Management at Yaveon, he is the expert for projects in a regulated environment. With almost 10 years of experience in highly regulated industries and more than 30 successfully implemented projects, he knows the key factors: stable processes and clear documentation.

For Max, quality is not a control instrument, but the key to success. He ensures that products and processes not only function smoothly, but are also quality audit and future-proof. With him and his team, customers get reliability and a partner who knows exactly what needs to be done.

It is important to him to know the needs of his customers and to speak the same language. He and his team see themselves as guides through the regulatory jungle.

"We support our customers in operating their systems efficiently and meeting the requirements of the regulated environment."

At Yaveon, Max shares his in-depth knowledge of compliance, process validation, GxP requirements and quality management. Always practical, solution-oriented and with the aim of helping companies achieve their goals efficiently and confidently.

Insights from Max Meidl

Good Manufacturing Practice (GMP)
Artikel
July 2025

Good Manufacturing Practice (GMP)

GMP summarizes all measures that ensure consistently high quality in the production and storage of medicinal products.

What is a quality audit? | Types, standards and more
Artikel
July 2025

What is a quality audit? | Types, standards and more

An audit is a systematic and documented quality management examination procedure carried out by auditors.

What is GAMP5? | Principles, process and more
Artikel
July 2025

What is GAMP5? | Principles, process and more

GAMP 5 is the guideline for ensuring the quality and compliance of automated systems in the pharmaceutical industry.

Good Distribution Practice (GDP)
Artikel
July 2025

Good Distribution Practice (GDP)

Good Distribution Practice (GDP) refers to the requirements for the distribution chain of medicinal products and the measures used to control it.

Everything about software validation
Artikel
July 2025

Everything about software validation

Software validation checks that software meets the requirements and is suitable for the intended purpose.

What is GxP and who sets the guidelines?
Artikel
July 2025

What is GxP and who sets the guidelines?

Gxp stands for "Good Practices" and refers to a collection of guidelines to ensure quality and compliance in the life sciences.

What is process validation and why is it important?
Artikel
July 2025

What is process validation and why is it important?

Process validation provides documented proof that a process delivers predefined results and does not pose a risk.

Supplier evaluation explained simply
Artikel
July 2025

Supplier evaluation explained simply

A supplier evaluation is a systematic process that enables companies to assess suppliers based on defined criteria.

We explain the validation of computer systems
Artikel
July 2025

We explain the validation of computer systems

Computer system validation describes a documented process that consistently ensures that software does what it was designed to do.

How to validate without stumbling blocks
Artikel
July 2025

How to validate without stumbling blocks

This article shows you how to master challenges and stumbling blocks in the process validation of computer systems with confidence.

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