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BioPharma Product Testing D/A/CH >> BioPharma Product Testing Services >> Analysis of Raw Materials

Analysis of Raw Materials, Active Ingredients and Excipients

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Our passion - Raw Material Testing!

No (bio-)pharmaceutical product can be manufactured without first determining the identity, purity and quality of its starting materials to ensure that the product is suitable for its intended use. If this critical step in the (bio-)pharmaceutical manufacturing process is successfully completed, costly production problems and delays can be avoided for you.

Eurofins BioPharma Product Testing Network of Laboratories has the wide range of know-how and state-of-the-art tools required to carry out all types of raw material testing, including the qualification of pharmacopoeia methods as well as the development, qualification and validation of new methods. No matter whether you need support in releasing your raw materials for production or for the qualification of your suppliers - we can advise and support you at the highest quality level.

Our analytical offer for you, ,some examples: 

  • Elemental analysis

  • Examination for residual solvents according to ICH Q3C, EP or USP

  • Harmonised microbial limits testing

  • Raw material testing for biologics, assessing the identity, purity, efficacy and quality of a variety of materials used in a wide variety of bioprocesses, using established GMP methods as well as tailor-made methods developed for individual customer needs.

  • Thermodynamic properties

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Aflatoxins are a group of mycotoxins and are natural substances produced by moulds and fungi that show toxic effects on humans and animals even in low concentrations. Over 20 naturally occurring aflatoxins are known, of which the aflatoxins B1, B2, G1, G2 and M1 are found in food. Typical food and feed are corn, rice, nuts, figs and other dried fruits or spices. Aflatoxins can also be very dangerous for people with weakened immune systems and therefore testing for aflatoxins in cannabis is a required test.

Contact us if you need to determine aflatoxins in your product.

We work worldwide with validated methods of the European Pharmacopoeia, EP, United States Pharmacopeia, USP, Japanese Pharmacopoeia, JP, British Pharmacopoeia, BP and ACS, FCC. If you miss a test because the monograph has changed, we can also fall back on a well-maintained archive. In addition to the conventional pharmacopoeias (including DAB, DAC, BP, JP), our library also contains the less common ones such as Chinese Pharmacopoeia, Ayurvedic Pharmacopoeia, Homeopathic Pharmacopoeia, Pharmacopoeia Helvetica.

Among other things, the determination of impurities with automated HPLC UV amino acid analyzers is one of our competencies. The EDQM has updated the relevant monographs by replacing the TLC method with a method for "ninhydrin-positive substances" and "ammonium". These methods allow an accurate calculation of amino acids impurities (caused by other amino acids), as well as a useful estimation of the content of ninhydrin-positive substances. Our analytical methods correspond exactly to the required EP monograph, analysis method 1, according to EP 2.2.56 and at the same time enable compliance with the specifications in EP 2.2.46.

We offer you the entire range of services related to the topic of "pharmaceutical glycerol". This includes tests according to EP, JP or USP. In addition, we offer you our help with all analytical questions in addition to chemical, microbiological and testing.

Pharmaglycerin is obtained from crude glycerin by simple, multi-stage processing (distillation, deodorization and filtration) and is commercially available in various purity grades. The 85% and 100% quality grades are specified in the pharmacopoeias with different purity criteria.

We can offer you the complete pharmaceutical-grade glycerol analytics according to all common pharmacopoeias.

  • Examination according to monographs
    • Properties
    • Identities
    • Degrees of purity
    • Water
    • Related substances and impurity A
    • Diethylene glycol and ethylene glycol
    • Content determination
  • Heavy metals screening using ICP-MS (ICH Q3D, USP, EP)
  • Viscosities (capillary viscometry and rotational viscometry)

The importance of screening for trace metal contamination (Trace Metals) is becoming increasingly important for the safety of bio-/pharmaceutical products. Eurofins BioPharma Product Testing DACH, in conjunction with our global network, offers almost all tests for the detection of metals and for a variety of applications that contribute to product safety, including active ingredient and raw material testing, cleaning validation, media screening, extractable/leachable studies and final product testing.

Karl Fischer titration has become one of the most widely used techniques for determining the water content in a variety of substances. Many pharmaceutical products contain water in adsorbed form, which is why determining water content is important to demonstrate compliance with regulatory standards.

Method transfer, method verification or validation according to ICH Q2 guidelines as well as method development are of course also possible with us. For this purpose, we have experts in all areas at our disposal worldwide, who communicate closely with each other on complex issues and to find the perfect solution to your question as quickly as possible.

Ensuring the high quality of sample processing

As GMP-certified service laboratories, adhering to the highest quality standards is our daily goal so that you receive high-quality analysis results from us. An incoming sample of your product is first checked for integrity and storage conditions and registered in our in-house Eurofins BioPharma Product Testin LIMS. From this point on, each sample vessel is unmistakably marked with a barcode. Each step is of course carried out in compliance with the 4-eye principle. On request, we will be happy to send you our template for a VAV. 

LabAccess.com, the secure and innovative online data access tool from Eurofins BioPharma Product Testing Network of Laboratories, gives you access to comprehensive laboratory information at any time during your ongoing project. With LabAccess.com, you can view information such as submitted samples, analyst noties, chromatograms, approved test results, certificates of analysis, raw data packages, and invoices online. 24 hours a day, 7 days a week.

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