Recipharm Wasserburger Arzneimittelwerk GmbH
Contract Manufacturers · Wasserburg am Inn
Recipharm Wasserburger Arzneimittelwerk GmbH is a contract manufacturer based in Wasserburg am Inn, Germany.
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Recipharm Wasserburger Arzneimittelwerk GmbH Overview
Recipharm Wasserburger Arzneimittelwerk GmbH is a contract manufacturer for pharmaceuticals or medical devices based in Wasserburg am Inn, Bavaria. The company produces on behalf of other companies and has a manufacturing license in accordance with Section 13 AMG.
Leistungen & Kapazitäten
Recipharm Wasserburger Arzneimittelwerk GmbH 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.
About Recipharm Wasserburger Arzneimittelwerk GmbH
Development and manufacturing solutions for solids, semi-solids and liquid dosage forms.
Location & Contact
Recipharm Wasserburger Arzneimittelwerk GmbH can be reached at the following address: Herderstraße 2, 83512 Wasserburg am Inn – Phone: 0807110080. For current information and enquiries, please contact the company directly.
More information: Lohnhersteller in Bayern or all Lohnhersteller in Germany on Sanoliste.
Contract Manufacturing in der Pharmaindustrie
Contract manufacturing organizations (CMOs) such as Recipharm Wasserburger Arzneimittelwerk GmbH produce medicines, 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, Recipharm Wasserburger Arzneimittelwerk GmbH 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 Bayern
Bavaria offers contract manufacturers such as Recipharm Wasserburger Arzneimittelwerk GmbH access to qualified specialists, a strong supplier industry and renowned pharmaceutical research institutions. The Wasserburg am Inn location enables short distances to clients and efficient logistics in the European internal market.
Frequently asked questions about Recipharm Wasserburger Arzneimittelwerk GmbH
What does Recipharm Wasserburger Arzneimittelwerk GmbH do?
Kompetenzzentrum für Lyophilisation und sterile Flüssigabfüllung, Teil der schwedischen Recipharm-Gruppe.
Where is Recipharm Wasserburger Arzneimittelwerk GmbH located?
Recipharm Wasserburger Arzneimittelwerk GmbH hat seinen Sitz in Wasserburg am Inn. Detaillierte Kontaktdaten, Adresse und Telefonnummer finden Sie auf dieser Seite.
In which field does Recipharm Wasserburger Arzneimittelwerk GmbH operate?
Recipharm Wasserburger Arzneimittelwerk GmbH 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. Recipharm Wasserburger Arzneimittelwerk GmbH 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.
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