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Quality made in Germany

Your reliable partner laboratory


In ChemCon you will find an internationally operating partner for the synthesis and analysis of pharmaceutical ingredients (APIs, GMP) and fine chemicals.

You are spot-on, if you are looking for a chemical substance (organic, inorganic, polymeric) in small to medium quantities. Examples are active pharmaceutical ingredients (APIs) in preclinical and clinical studies or for commercial chemical and pharmaceutical application.

ChemCon’s analytics team takes care of your inquiries if you are looking for ICH-compliant quality control, GMP validation, release analysis, impurity determination, reference standards or answers to other analytical queries.

On top of our chemical services, you will also find selected products in ChemCon’s portfolio.

Quality assurance and regulatory consulting completes comprehensive GMP-compliant production and analysis, validation and documentation.

Contract development and manufacturing organization (CDMO)

Customized synthesis and process development
Organic and inorganic chemistry
Polymer Chemistry
Technical batches and GMP pilot batches
Active substances for clinical studies
Fine Chemicals
Cytotoxic, highly potent or BtMG regulated compounds
Close communication with chemists and process engineers


Chemical Expertise

Small but important? Kilolab services availabe for commercial supply

Commercial contract manufacturing


We enable commercial routine production for an annual requirement of < 100 g to several 100 kg.

Your pharmaceutical ingredients are produced to GMP guidelines and your specifications for application in injectable, ophthalmic, oral, or topic formulations.

 

We also produce chemicals, starting materials, or reference standards upon inquiry. Our analytics team takes care of qualification and release for you.

Chemical testing services

Chemical characterization
Quality control
Impurity determination
Method development and validation
Release analysis
Stability studies
Reference standards

Close, outcome-oriented communication: We also work with you on challenges, where routine testing is not sufficient.

What we can do for you

Quality confirmed by FDA and German authorities

Audits and GMP inspections


Since founding in 1997, ChemCon has been audited over 200 times, to the full satisfaction of the customers. We are looking back onto a long list of successful GMP inspections, most recently 2018 by the FDA (US Food and Drug Administration) and 2019 by German authorities (Regierungspräsidium Tübingen, EU GMP)

 

Inspection History

About ChemCon

News & Events


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News
New ChemCon cleanroom.
News

The new advanced cleanroom facility at ChemCon is now operational!

With an investment of 6 million euros, ChemCon GmbH has expanded its production capacities

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CPHI Worldwide in Milan
Events

ChemCon at CPHI Worldwide 2024 in Milan

ChemCon will attend CPHI Worldwide.

08.-10, Oktober, Mailand, Italien

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NLS Days Malmö
Events

ChemCon at the NLS Days

ChemCon will participate at the NLS Days.

September 18-19, Malmö, Sweden

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Chemspec Europe 2024
Events

ChemCon at Chemspec Europe 2024

ChemCon will participate at Chemspec Europe 2024. June 19 to 20, Düsseldorf.

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