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.

Wendlingen Am Neckar · Baden-Württemberg

AGON Pharma GmbH, based in Wendlingen, provides contract analytical services for batch release testing, stability studies in climatic chambers, and method validation and marketing authorisation support for medicinal products of other companies.

Hamburg-Altstadt · Hamburg

Based in Hamburg, provides pharmaceutical companies with EU marketing authorisation procedures, import services and Qualified Person batch certification. The company also markets its own medicinal products, including Alltrevo, Hialurom and Rafaject.

Köln

Based in Cologne, is a contract research organisation (CRO) serving small and medium-sized biopharmaceutical companies. It offers clinical development, pharmacovigilance and regulatory consulting.

Lüchow (wendland) · Niedersachsen

Ismaning

Is part of the Astrum Group, headquartered in Madrid. The company provides clinical trials from Phase I to Phase IV, along with advisory services on development strategy and dealings with regulatory authorities.

Baesweiler · Nordrhein-Westfalen

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.

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.

München · Bayern

Based in München, brokers active pharmaceutical ingredients and finished medicinal products and offers laboratory testing in Marseille, regulatory support for manufacturers' dossiers, and logistics with cGMP-compliant warehousing.

München

Based in Munich, is a consultancy for drug development that also provides clinical trial supply. It supports pharmaceutical and biotechnology companies on strategic matters and handles the packaging, labelling, storage and distribution of trial medication.

Frankfurt

Based in Frankfurt, is part of the global CRO Linical and provides clinical contract research, project management and regulatory affairs consultancy to biopharmaceutical companies.

Oberhaching · Bayern

Based in Oberhaching near Munich, manufactures lyophilised and liquid sterile products, predominantly for the hospital market. The company also prepares marketing authorisation dossiers and periodic reports.

Hannover

Based in Hannover, is an independent contract research organisation (CRO) providing clinical trial services, regulatory affairs, data management and pharmacovigilance to pharmaceutical and biotechnology companies.

Ingelheim Am Rhein · Rheinland-Pfalz

Based in Ingelheim am Rhein, is a medium-sized pharmaceutical company that develops and manufactures active pharmaceutical ingredients and intermediates on a contract basis. It also offers regulatory and quality services.

Landau In Der Pfalz · Rheinland-Pfalz

Based in Landau in der Pfalz, advises pharmaceutical companies on regulatory affairs, marketing authorisation dossiers and project evaluation across the entire medicinal product lifecycle.

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.

Münster

Is part of the Symbio Group, a CRO for clinical trials in dermatology, aesthetics, gastroenterology and inflammatory diseases.

Muenster · Nordrhein-Westfalen

Based in Münster with a site in Planegg, advises life sciences companies on regulatory affairs, quality management and pharmacovigilance. Its services also include the external assumption of the Qualified Person (QP) and Qualified Person for Pharmacovigilance (QPPV) roles.

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.

Frechen

Based in Frechen near Cologne, is an independent CRO for clinical trials from Phase I to Phase IV and for non-interventional studies, offering biometrics, data management, monitoring and marketing authorisation support.

Berlin

Based in Berlin, advises manufacturers of natural health products on marketing authorisation dossiers in Europe and conducts clinical studies. Founded in 2001, the company employs around 40 staff and operates its own study centre.