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160 pharmaceutical service providers with evidence

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A&O Pharma GmbH

Efringen-Kirchen

✓ Manufacturing authorisation✓ GMP certificate

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.

Contract analytical testingAnalytical method development and validationExternal QP and batch certificationGMP audits and supplier qualification +4

Allucent (DE) GmbH

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.

Regulatory affairsPharmacovigilanceContract research organisation (CRO)

Diapharm GmbH & Co. KG

Muenster · Nordrhein-Westfalen

✓ Manufacturing authorisation✓ GMP certificate

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.

External QP and batch certificationGMP audits and supplier qualificationQM and GMP consultingPharmacovigilance

Evidenze GmbH

Essen

Based in Essen, is a contract research and consultancy company for clinical trials, with a focus on study management, data management, biostatistics, pharmacovigilance and quality assurance audits.

PharmacovigilanceContract research organisation (CRO)Computer system validation (CSV)

Lyomark Pharma GmbH

Oberhaching · Bayern

✓ Manufacturing authorisation✓ GMP certificate

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.

Contract manufacturing of sterile productsRegulatory affairsPharmacovigilance

Mediconomics GmbH

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.

Regulatory affairsPharmacovigilanceContract research organisation (CRO)

TentaConsult Pharma & Med GmbH

Muenster · Nordrhein-Westfalen

✓ Manufacturing authorisation✓ GMP certificate

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.

External QP and batch certificationGMP audits and supplier qualificationRegulatory affairsPharmacovigilance