Advanced analytics for the highest demands
Precision and innovation in drug analysis
In the pharmaceutical industry, SAS Hagmann offers specialized analytical services that are crucial for the development and quality assurance of medications. Our portfolio includes active ingredient analysis, stability testing, and purity controls to ensure the efficacy, safety, and purity of pharmaceutical products.
Using state-of-the-art technologies and in-depth expertise, we assist our clients in meeting stringent regulatory requirements and maintaining the highest quality standards.
About SAS hagmann: Pioneers in analytical chemistry
Since our founding in 1996, SAS hagmann has established itself as an independent, family-run contract laboratory for analytical chemistry.
Our goal is your satisfaction. We support you with our many years of experience in quality control, validation and monitoring of processes as well as the analysis of residues on implants and the identification of contamination on surfaces. Our team of experts helps you to meet the high quality requirements in industries such as automotive, aviation, pharmaceuticals and medical technology.
At SAS hagmann, the passion for chemical analysis is at the heart of our work.
Key procedures at a glance
Active Ingredient Analysis
SAS Hagmann supports clients in conducting Environmental Risk Assessments (ERA) as required for the approval processes of pharmaceuticals according to the European Medicines Agency (EMA) standards. A registration dossier for the market authorization of human medicinal products (HMP) must mandatorily include an ERA, which evaluates the intended use in the dosage form, the physicochemical and ecotoxicological properties, and the environmental behavior of the active ingredient.
The necessary risk assessment is divided into phases, during which chemical and biological analyses are conducted according to widely recognized OECD protocols.
In addition to sampling the actual pharmaceutical active ingredients (API), SAS Hagmann assists clients in implementing risk management measures such as ICH Q3, which aim to evaluate the entire pharmaceutical product, including not only the active ingredients but also excipients, precursor compounds, and other process-involved reagents.
Our contact persons
Contact us, and we will help you find the information you need and provide you with customized solutions for your specific requirements.
Pharmaceutical
Selina Steinhilber
M.Sc. Biomedical Sciences
- QMB
- Project Manager Medical Products
The chemistry must be right. You give your trust, we give our responsibility.
Trusted Partner
Trust is the foundation of every partnership – and at SAS Hagmann, we build on decades of proven reliability. Our customers value us as a trusted partner because we consistently deliver transparent and traceable results. With us, you have a partner by your side who combines integrity and expertise in every step.
Customized Solutions
Every project is unique and deserves a customized solution. SAS Hagmann stands for individual analytics precisely tailored to your specific requirements. Our approach is not just to provide data, but solutions that perfectly fit and advance your project.
Innovative Technology
Innovation drives us to constantly push the boundaries of what is possible. We continuously invest in cutting-edge technologies and methods to provide you with advanced analytical services. We combine the latest scientific insights with proven procedures to guarantee results that pave the way for the future.
Customized solutions
Customized solutions for new challenges are our specialty. Where others see problems, we deliver results for our clients because when precision matters, businesses rely on SAS Hagmann. Contact us now and let’s work together on your challenge.
Dr. Nikolas Pietrzik
Graduate Chemist
SAS Hagmann GmbH & Co. KG, founded in 1996, is an independent, family-owned analytical contract laboratory located in Horb am Neckar, Germany. The company is dedicated to customer satisfaction and supports them with extensive experience in various areas:
- Quality control for incoming and outgoing goods
- Validation and monitoring of processes
- Surface analysis and residue detection for implants and medical devices
- Development of analysis strategies (and concepts) within risk management
- Substance identification for approval processes of products such as pharmaceuticals, biocides, chemicals, cosmetics, etc.
Every question is the first step towards a new solution.
We are just a click away to answer your questions and provide you with our expertise. Fill out the contact form, and a member of our team will promptly get in touch with you. At SAS Hagmann, we are ready to listen and collaborate on solutions that truly make a difference.
