Laboratory services & pharmaceutical analysis
We are your partner for pharmaceutical analysis and quality control.
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Pharmaceutical analysis: range of services
With more than 30 years of experience and our continual quest for improvement, we provide analytical laboratory services of the highest level for active ingredients, excipients, medicinal products and drug-related products. In addition to developing and validating analytical methods, batch release analysis, stability testing and structure determination of unknown substances, our core expertise also includes risk-based and solutions-oriented client consulting.
Our analytical laboratories are staffed by more than 45 highly skilled professionels who are dedicated to meeting your needs in a focused and efficient manner. Our interdisciplinary teams and professional project management ensure the success of even the most complex projects. Our GMP and FDA certifications as well as a manufacturing authorisation for the release of clinical and market batches underline our commitment to quality.
An overview of our technological equipment can be found here: Equipment Laboratory Services
Pharmaceutical analysis: Comprehensive advice from experts
Our consulting services cover analytical issues for human and veterinary medicinal products as well as for medical devices and combination products in accordance with current regulatory requirements. Our services include:
- Review of specifications, analytical methods and validation reports
- Planning and implementation of analytical method transfers and production validations
- Gap analysis of analytical and technological documents in the context of the development and authorisation of medicinal products
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Laboratory services for active ingredients, excipients, finished dosage forms, medical devices
As experts with many years of experience, we work with the full range of pharmaceutical dosage forms and have extensive knowledge of the effects of the matrix on the availability and stability of active ingredients.
We test active ingredients and excipients according to the latest monographs of Ph. Eur., USP and other pharmacopoeias. For new active ingredients and excipients, we develop and validate analytical methods to test for content and purity using cutting-edge analytical technologies. This includes the testing of highly potent active ingredients or narcotics.
Our laboratory team has many years of experience in developing and validating test methods and their application to different dosage forms.
When developing test methods, we pay particular attention to efficient an robust sample preparation. Our experience includes a wide range of complex matrices such as semi-solid and prolonged-release formulations.
Our comprehensive range of chemical and physical test equipment enables us to investigate products containing chemically defined herbal and biotechnologically active ingredients.
As specialists in analytical testing and quality control of substance-based medical devices and drug-device combination products, we can develop and validate various test methods, e.g. for identity testing, content determination, purity testing and the release of active pharmaceutical ingredients in combination products in accordance with national and international guidelines. For quality control, analytical testing for batch release and shelf life are carried out according to defined specifications.
For the tests required as part of the biocompatibility requirements in accordance with ISO 10993, we can offer a tailor-made chemical-physical characterisation concept for your product and perform the extraction studies in our laboratory.
Technical equipment
Gallery of the technical equipment in our labs: The technical equipment of our laboratories includes chromatographic methods (HPLC, GC, TLC), LC-MS, GC-MS, electrophoresis, ASS, IR, photometry, dissolution, relevant test methods for biological molecules as well as wet chemical methods.