Zamann Pharma Support logo

Siedlerstraße 7 | 68623 Lampertheim, Germany

info@zamann-pharma.com

Request an appointment now

Towards Quality
Excellence

Zamann Pharma Support assists you in the digital evolution of your company into a quality and process-driven enterprise.

Our solutions for your company

Zamann supports small, medium and global-sized companies in digitalization, compliance and scalable quality management.

We are fully specialized in Life Science Quality Consultancy services and solutions. As strong partners of the pharmaceutical and medical device industry we support companies in the following topics:

Training and Coaching of employees 

Management Consultation 

Global Project Management 

cGxP Compliance 

Software development for Pharma 

Validation and Qualification 

Professionals discussing about Quality Management System, representing Zamann's global project services

Global Project Management Learn more 

Quality consultant analyzing data for compliance, representing Zamann's Quality Consultancy service.

Quality Consultancy Learn more 

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Digitalization Learn more 

Focused professional woman with crossed arms attending a validation and qualification meeting, representing Zamann's expertise in the area

Validation and Qualification Learn more 

How does a collaboration work?

Collaboration is all about understanding and addressing your unique needs.

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1. Appointment request

You request a free initial consultation via our website and answer a few questions.

2. Preliminary talk

One of our employees will talk to you over the phone about your request and put you in touch with the right contact person.

3. Virtual consultation

A strategy consultant will give you 60 minutes of individual advice on your situation and work with you to develop a solution to your problem.

4. Long-term cooperation

After the initial consultation, there is the option of us supporting you in the long-term implementation of your solution.

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4950

trees planted

4.72

hectares reforested

995

tonnes CO2 captured

Tree-Nation

Sustainability is a core segment of the Zamann company culture and part of every single onboarding program for our employees. Also, we simply love planting trees around the world.

TÜV SÜD ISO 9001 Quality Management System certification emblem for excellence in quality assurance standards.

TÜV-certified
ISO 9001 Quality Management System

Icon representing consulting services in pharmacy and medical technology quality assurance.

Consulting service in the field of pharmacy, medical technology and quality assurance

Icon for supplier qualification services in pharmacy and medical technology sectors

Supplier qualification in the field of pharmacy, medical technology and quality assurance. 

Icon depicting personnel qualification in the field of pharmacy, medical technology, and quality assurance.

Personnel qualification in the field of pharmacy, medical technology and quality assurance. 

Icon illustrating customer-specific quality management system solutions

Customer-specific provision of quality management systems.

Our Customers

Phoenix Pharma
LabWare
BA Unternehmensgruppe
Reckitt
BIONTECH
ratiopharm
SANOFI
Boehringer Ingelheim
Biotest
Heraeus
Takeda
HAYS
UMM

What people think about us

[grw id="624"]
James
James1 review
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Alles Top!
Kurz und knapp: Kann Zamann und Alis Team nur vollkommenempfehlen. Arbeiten schon mehrere Jahre mit der Firma in diversen GMP Themen zusammen und haben ausschließlich positives zu berichten. Fachlich, als auch menschlich. Zamann hat in unserer Firmengruppe die anderen „big four“ quasi im Alleingang verdrängt. Danke und bis zum nächsten Meeting
Date of experience: October 28, 2023
Burl
Burl1 review
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verified
CSV Assessments
Im Vorfeld eines bevorstehenden Audits standen wir vor der Herausforderung, unsere verschiedenen Systeme zu bewerten. Dank des CSV GAP Assessments von Zamann konnten wir uns optimal vorbereiten. Sie haben nicht nur Schwachstellen identifiziert, sondern auch präzise Lösungsvorschläge geliefert. Ihre systematische Herangehensweise hat uns dabei geholfen, sicherzustellen, dass wir für das Audit bestens gerüstet sind. Zamann war wertvoller Partner in anstrengenden Zeiten.
Date of experience: October 28, 2023
Thomas
Thomas1 review
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SOPs
Zamann erstellte klare SOPs, die unsere komplexen Aufgaben vereinfachten und unser Firmen Know-How endlich Mal auf Papier ficxierten. Jedes Verfahren hat jetzt eine deutliche Richtlinie, wodurch unsere tägliche Arbeit flüssiger und effizienter geworden ist. Ein großes Lob für ihre Unterstützung!
Date of experience: October 25, 2023
Betty
Betty1 review
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verified
GAP Assessment for a global system
Zamann didn't just skim the surface; they delved deep, highlighting nuances we might have missed . Every gap was not only identified but also paired with thoughtful strategies for improvement. With their holistic approach they provided our company an opportunity to avoid potential audit findings. Zamann didn't just show us where we stood; they illuminated the path forward. Their contribution has been invaluable in refining our CSV processes.
Date of experience: October 23, 2023
Connie
Connie1 review
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verified
Merging IT principles with GMP…
Merging IT principles with GMP standards is no small feat, but with Zamann, this challenge transformed into an opportunity. Under Marcos's leadership, the team crafted tailored software and database solutions that perfectly fit our laboratory's distinct requirements. Their approach was not just about providing support, but about delivering innovative, compliant solutions. We want to say thank you to the entire Zamann team!
Date of experience: October 21, 2023
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The newest Pharma Reports of Zamann Pharma Support

We regularly report about our hands-on compliance experiences

ICH M7 for Nitrosamines: Steps for a Lifecycle Management

ICH Guideline M7 provides a solid framework for the management of nitrosamines in medicinal products. By following these guidelines and implementing a comprehensive lifecycle management approach, pharmaceutical companies can effectively minimize the risks associated with nitrosamine impurities. This ensures the

Getting Started with Process Validation

Learn the fundamental steps and best practices for successful Process Validation in manufacturing, covering design, qualification, and continuous monitoring to ensure product quality and compliance.

Important Questionnaire for Nitrosamine Risk Assessment for API

The Nitrosamine Risk Assessment Questionnaire for APIs is an indispensable tool for pharmaceutical manufacturers. It provides a structured approach to identifying potential sources of nitrosamine contamination and implementing effective mitigation strategies.

Smart SOPs: AI Transforming SOP Management

In the pharmaceutical industry, managing Standard Operating Procedures (SOPs) is increasingly complex due to regulatory demands. This article highlights the challenges of SOP retrieval and showcases how the AI-driven Zamann Retrieval Augmented System (ZaRAS) transforms SOP management through enhanced efficiency,

Are Nitrosamines Hiding in Your Food? Tips to Avoid Them

Understanding the conditions that lead to nitrosamine formation is crucial for reducing their presence in our food. This article explores the science behind nitrosamine formation in cured meats and offers practical tips for minimizing their levels, ensuring a safer and

IVD QA: Regulations & Testing Methods

In the world of diagnostics, accuracy is paramount. For In Vitro Diagnostics (IVD) used in countless medical procedures, robust Quality Assurance (QA) practices are essential. These procedures ensure compliance with specific regulations and rigorous testing methods. The

Performance Qualification: A Step-by-Step Guide for Pharma Experts

Performance Qualification (PQ) is a vital process in the pharmaceutical industry, ensuring that equipment operates effectively under real-world conditions. This guide walks you through the essential steps to perform PQ, from writing a robust protocol to meeting FDA requirements. Explore

Top 10 Steps for Qualifying a New GMP Facility

The qualification of a GMP facility is essential to ensure the high standards of pharmaceutical production and to guarantee product quality. In our latest article, you will learn the 10 most important steps for the successful qualification of a new

NDSRI Regulatory reporting requirements and their timeline

Navigating NDSRI regulatory reporting requirements is crucial for pharmaceutical companies to ensure compliance and patient safety. These regulations mandate timely and accurate reporting of nitrosamine impurities in medicines. Understanding the timeline for these requirements helps streamline processes and avoid costly
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We strive for customer success.

Zamann is constantly looking for new talents with the right team and performance spirit to support us in our mission.

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