Artesan Pharma GmbH & Co. KG

Contract Manufacturers · Lüchow

Artesan Pharma GmbH & Co. KG is a contract manufacturer based in Lüchow, Germany.

Content in German

The detailed company information on this page is provided in the original German language. You can use your browser's built-in translation feature to view it in English.

Right-click on the page and select "Translate to English" or use the translation icon in your browser's address bar.

Artesan Pharma GmbH & Co. KG – Address & Contact

Address

Wendlandstraße 1
29439 Lüchow

Artesan Pharma GmbH & Co. KG Overview

Artesan Pharma GmbH & Co. KG is a contract manufacturer for pharmaceuticals or medical devices based in Lüchow, Lower Saxony. The company produces on behalf of other companies and has a manufacturing license in accordance with Section 13 AMG.

Leistungen & Kapazitäten

Artesan Pharma GmbH & Co. KG offers contract manufacturing services for pharmaceuticals and/or medical devices. This typically includes synthesis, formulation, filling, packaging and quality control. All processes take place under GMP-compliant conditions.

Location & Contact

Artesan Pharma GmbH & Co. KG can be reached at the following address: Wendlandstraße 1, 29439 Lüchow – Phone: 058419390. For current information and enquiries, please contact the company directly.

More information: Lohnhersteller in Niedersachsen or all Lohnhersteller in Germany on Sanoliste.

Contract Manufacturing in der Pharmaindustrie

Contract manufacturing organizations (CMOs) such as Artesan Pharma GmbH & Co. KG produce pharmaceuticals, dietary supplements or medical devices on behalf of other companies. Contract manufacturing typically includes active ingredient synthesis, formulation, filling, primary and secondary packaging through to release by a qualified person (QP). The CMO market is growing worldwide as more and more pharmaceutical companies outsource production to specialized partners.

GMP-Anforderungen & Herstellungserlaubnis

As a contract manufacturer, Artesan Pharma GmbH & Co. KG requires a manufacturing permit in accordance with Section 13 AMG. Production must comply with the rules of Good Manufacturing Practice (GMP), which are defined in the EU by EudraLex Volume 4. Regular inspections by the responsible state authority and a comprehensive quality management system are mandatory. Each batch is checked by a qualified person (QP) before release.

Standortvorteil Niedersachsen

Lower Saxony offers contract manufacturers such as Artesan Pharma GmbH & Co. KG access to qualified specialists, a strong supplier industry and renowned pharmaceutical research institutions. The Lüchow location enables short distances to clients and efficient logistics in the European internal market.

Frequently asked questions about Artesan Pharma GmbH & Co. KG

What does Artesan Pharma GmbH & Co. KG do?

Pharmazeutischer Lohnhersteller für feste Darreichungsformen, Lutschpastillen und Flüssigkeiten.

Where is Artesan Pharma GmbH & Co. KG located?

Artesan Pharma GmbH & Co. KG hat seinen Sitz in Lüchow. Detaillierte Kontaktdaten, Adresse und Telefonnummer finden Sie auf dieser Seite.

In which field does Artesan Pharma GmbH & Co. KG operate?

Artesan Pharma GmbH & Co. KG ist in der Lohnhersteller-Branche tätig und bietet spezialisierte Produkte und Dienstleistungen für das Gesundheitswesen an.

What is the difference between a CMO and a CDMO?

A CMO (Contract Manufacturing Organization) exclusively carries out contract manufacturing. A CDMO (Contract Development and Manufacturing Organization) additionally offers development services \u2013 from formulation development through scale-up to process validation. Artesan Pharma GmbH & Co. KG operates as a contract manufacturer in this market.

What is a Qualified Person (QP)?

The Qualified Person (QP) is an expert required by law under Section 14 of the German Medicines Act (AMG) who inspects and releases each batch of medicines before it is placed on the market. The QP bears personal responsibility for ensuring that each batch has been manufactured and tested in accordance with GMP.

What certifications does a contract manufacturer require?

Contract manufacturers require a manufacturing licence pursuant to Section 13 of the German Medicines Act (AMG), a GMP certificate based on regular authority inspections and, depending on the client, additional certifications such as ISO 9001, ISO 13485 (for medical devices) or FDA registration for the US market.

Artesan Pharma GmbH & Co. KG on social media

Contract Manufacturers in Niedersachsen

All Contract Manufacturers in Niedersachsen on Sanoliste — or discover all categories by federal state.

Last updated: 17.03.2026 · Category: Contract Manufacturers