High-quality pharmaceutical starting materials are a key factor in ensuring the safety of drug therapies. To guarantee this, analytical testing of active ingredients and drugs in accordance with international quality standards is essential and forms the basis for safe and successful therapy. As a GMP-certified contract laboratory, QMEDIS Analytics GmbH offers everything necessary to meet the ever-growing quality demands in the pharmaceutical sector.
Our range of services
We rely on a broad spectrum of methods to ensure customized analyses for your requirements:
- Chromatographic methods: HPLC (high-performance liquid chromatography), GC (gas chromatography), and TLC (thin-layer chromatography)
- Spectroscopic methods: MIR (mid-IR), NIR (near-infrared), UV/Vis spectroscopy
- Physical measurements: densimeter and refractometer measurements
Our portfolio – analytics at the highest level
- Pharmacopoeia analytics: performance of standardized tests in accordance with current European and international monographs (e.g., Ph. Eur., DAB, USP)
- Method development, validation, and transfer: Development of individual, standard-compliant analysis methods as well as their validation and smooth transfer
- Routine release analysis: Reliable and timely analyses to support your batch release processes
- Analytical project support for stability studies
With our experienced team and state-of-the-art equipment, we offer customized analytical solutions tailored to your needs—from routine testing and stability studies to method development and validation—ensuring that your products meet the highest quality standards—efficiently, compliantly, and with the utmost care.
Thanks to our expertise, we are a reliable partner for pharmaceutical companies, active ingredient manufacturers, and pharmacies that value quality, innovation, and drug therapy safety.
QMEDIS Analytics GmbH – your partner for precise analytics and sustainable quality assurance.