Providers

Efringen-Kirchen

Based in Efringen-Kirchen with sites in Itzehoe and Lörrach, provides service support to pharmaceutical companies, including batch certification by Qualified Persons, regulatory affairs, GMP consulting and GMP-certified analytics.

Neustadt · Hamburg

Based in Hamburg and Dassow, manufactures its own oncology generics and advises contract manufacturers on EU GMP compliance. The company also offers a mobile cleanroom container.

Köln · Nordrhein-Westfalen

Based in Köln, develops cannabinoid-based medicinal products and cannabis genetics. The company offers genetic licences, propagation material and consultancy on GMP licences.

Adlershof · Berlin

Based in Berlin-Adlershof, develops and validates chromatographic analytical methods under Quality by Design (QbD) principles and analyses impurities for clients. The company also carries out GMP audits at contract laboratories.

Aachen

Based in Aachen, is part of a US-based full-service CRO headquartered in Horsham. The company supports pharmaceutical and biotech firms with clinical trials, marketing authorisation and quality management.

Muenster · Nordrhein-Westfalen

Based in Münster, advises pharmaceutical companies on regulatory affairs, GMP quality management and pharmacovigilance, and also assumes responsibility functions such as acting as an external Qualified Person.

Bad Salzungen · Thüringen

Based in Bad Salzungen, provides quality management and regulatory consulting for medicinal products, particularly narcotic drugs and medicinal cannabis, and also markets its own cannabis products.

Limburg · Hessen

Based in Limburg an der Lahn, advises pharmaceutical and life science companies on strategy, M&A, supply chain and quality management. Its partners bring between 15 and 35 years of industry experience.

Bensheim · Hessen

Has been an independent service provider for pharmaceutical development and marketing authorisation since 1994. The company supports production and batch certification at contract manufacturers, as well as quality systems and regulatory inspections.

München · Bayern

Based in München and Lörrach, advises the pharmaceutical industry on GMP, GDP and ISO 13485, provides Qualified Persons for batch certification, and carries out audits. The company also offers storage, primary packaging and labelling services.

Siek · Schleswig-Holstein

Distributes pharmaceutical active ingredients worldwide, offering sourcing, qualification of active ingredient manufacturers, GMP-compliant storage and regulatory support such as the preparation of Drug Master Files.

Mannheim

Is a clinical research organisation focusing on human challenge studies, Phase I to III trials and laboratory analytics. It also offers PK/PD analysis, biobanking and quality management for studies.

Leimen · Baden-Württemberg

Based in Leimen, provides analytical services for the pharmaceutical industry, including method development and validation, stability and release testing, and consultancy on Quality by Design.