GMP Compliance Insights & Professional Perspectives
Blog
Blog Overview
The following articles provide structured insights and professional reflections on Good Manufacturing Practice (GMP), audit readiness, data integrity, quality system design, and other compliance-relevant topics.
Content is presented in English and aimed at quality professionals, compliance teams, and decision makers in regulated environments. Articles are intended to promote practical understanding and contextual clarity, not to prescribe specific solutions.
Published content may range from distilled regulatory perspectives to pragmatic process considerations.
GMP Explained: What GMP Really Means in Daily Practice
GMP Explained: What GMP Really Means in Daily Practice
Introduction
GMP is often reduced to documentation, SOPs, and inspection readiness.
Many professionals work for years in GMP environments and still struggle to explain what GMP actually means.
In daily practice, GMP is neither abstract nor theoretical.
It is visible — every day — in decisions, responsibilities, and how systems are used under real conditions.
This article is part of my “GMP Explained” series, created to clarify what GMP really is — and what it is not.
Your Start in the GMP World: The 5 Essential Steps for New Companies
Entering the regulated GMP sector often feels like diving into the deep end for small and medium-sized enterprises. Without a large compliance department, you might wonder where to begin and how to meet complex requirements. But don't worry, it's absolutely manageable.
From my many years of experience working with companies just like yours, I know that success depends on setting the right course from the outset. I want to show you the five most important steps to build a solid foundation and avoid typical beginner's mistakes.