Remexian Pharma GmbH
Pharmaceutical Companies · Teltow-Fläming
Remexian Pharma GmbH is a pharmaceutical company based in Teltow-Fläming, Berlin, Germany. The company operates in the German pharmaceutical market and is regulated by the BfArM (Federal Institute for Drugs and Medical Devices).
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Remexian Pharma GmbH – Address & Contact
Remexian Pharma GmbH Overview
Remexian Pharma GmbH is a pharmaceutical company based in Teltow-Fläming, Berlin. The company operates in the German pharmaceutical market and is regulated by the BfArM (Federal Institute for Drugs and Medical Devices).
Activities & Products
Pharmaceutical companies such as Remexian Pharma GmbH develop, produce or distribute medicines for the German and international market. All authorised products are subject to approval and are regulated by BfArM or the European Medicines Agency (EMA).
About Remexian Pharma GmbH
Wir glauben, thes jedem Patienten the the best possible Behofdlung zusteht. Unsere zentrale Antriebskraft is the Wohlergehen the Patienten im Kampf gegen Krofkheiten.
Location & Contact
Remexian Pharma GmbH can be reached at the following address: Märkersteig 27, 14974 Teltow-Fläming – Phone: 033785159310. For current information and enquiries, please contact the company directly.
More information: Pharmaunternehmen in Berlin or all Pharmaunternehmen in Germany on Sanoliste.
Pharmazeutische Regulierung in Deutschland
Pharmaceutical companies such as Remexian Pharma GmbH are subject to one of the world's most stringent regulatory frameworks in Germany. The German Medicinal Products Act (AMG) governs the authorisation, manufacturing, distribution and monitoring of medicinal products. Market authorisation for new active substances falls under the responsibility of either the Federal Institute for Drugs and Medical Devices (BfArM) or the European Medicines Agency (EMA), depending on whether a national or centralised authorisation is sought.
Arzneimittelversorgung & Marktumfeld
With a revenue volume exceeding 50 billion euros, the German pharmaceutical market is one of the largest in Europe. Remexian Pharma GmbH, based in Teltow-Fläming, is part of this market. The supply chain from manufacturer through wholesaler to pharmacy is governed by Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP). Since the entry into force of the Act for Greater Safety in the Medicinal Products Supply (GSAV), stricter requirements for the traceability of medicinal products also apply.
Pharmastandort Berlin
Berlin is a significant pharmaceutical location in Germany. Companies such as Remexian Pharma GmbH benefit from proximity to research institutions, university hospitals and well-developed infrastructure. The industry employs over 140,000 people in Germany and invests billions annually in research and development.
Frequently asked questions about Remexian Pharma GmbH
What does Remexian Pharma GmbH do?
Remexian Pharma GmbH betreibt als pharmazeutisches company den Import of medizinischem Cannabis, the in Europa produces is. Es sorgt for möglichst kurze Lieferwege and tritt also als Großhändler on. Handelsware is the getrocknete Blüte the Hanfpflanze.
What medicines does Remexian Pharma GmbH manufacture?
Remexian Pharma GmbH is a pharmaceutical company in Teltow-Fläming. Über Remexian Pharma GmbH Remexian Pharma GmbH is ein biopharmazeutisches company, the sich on the development and Vermarktung of innovativen Medikamenten and Therapien kon Alle in Germany zugelassenen medicines are in the medicines-Datenbank des BfArM recherchierbar.
How are medicines approved in Germany?
Neue medicines benötigen vor dem Inverkehrbringen eine Zulassung durch the BfArM (national) or the EMA (europaweit). Der Zulassungsprozess umfasst the Prüfung of quality, Wirksamkeit and Unbedenklichkeit on Basis präklinischer and klinischer Stuthen. Die Nutzenbewertung after § 35a SGB V entscheidet about the Erstattung durch the gesetzlichen Krankenkassen.
What does GMP mean in pharmaceutical production?
GMP (Good Manufacturing Practice) bezeichnet the Gute manufacturingspraxis – ein System of qualitysstandards, the sicherstellt, thes medicines gleichbleibend after den gefortheten qualitysnormen hergestellt and geprüft are. Die GMP-Richtlinien are in the EU durch den EudraLex Volume 4 definiert.
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