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Pharmaceutical Testing

Our pharmaceutical testing laboratory – holding a GMP certificate – undertakes quality assurance analysis for pharmaceutical drug products and starting materials as an independent European verification site.

Services

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Chemical and physical tests

Our range of analyses covers a broad spectrum of chemical and physical tests for pharmaceutical products. In addition to routine quality control tests, our experts also perform the development and validation of procedures for customer-specific requests.

Quality control

Our laboratories' most important partners are pharmaceutical companies, manufacturers of active pharmaceutical ingredients and wholesalers. We provide our customers with fast, professional and reliable services in the fields of chemical and physical quality control and microbiological testing.

EU retesting and product release

Providing analytical and quality assurance services for the entry of imported pharmaceutical products into the European Union market. Quality assurance of the entire pharmaceutical supply chain, from the manufacturer of the active ingredient to the EU receiving warehouse of the finished product.

Audits

We can perform audits of the entire pharmaceutical supply chain (suppliers, contract manufacturers, etc.) on the basis of international or customer requirements on the following quality systems.

Solving special cases

Our comprehensive instrumentation allows us to offer our clients a complete service from a single source. International and interdisciplinary collaboration allows us to deliver our analyses quickly and flexibly.

Microbiological tests on sterile product

We provide our customers with fast, professional and reliable services in the field of chemical and physical quality control and microbiological testing. Pharmaceutical raw materials and finished products are tested under GMP conditions. Sterile and non-sterile preparations are tested in various...

Nitrosamine contamination testing

Nitrosamine contamination testing is performed by HPLC MS-MS on finished products and active ingredients. After analytical method development, the analytical method is validated according to current guidelines and customer requirements.

PSS Insourcing Solutions®

We strategically partner with clients at their site to drive quality, innovation, and operational excellence for great results. That’s the power of PSS®.

Extractables & Leachables

Extractables and leachables (E&L) studies enable drug sponsors to quantify and identify the risks of potentially toxic leachable impurities migrating into a drug solution from container closure systems, processing equipment or packaging.

Our company in numbers

450000000

Examination annually

200000

Analytical method

61000

Number of employees