Fareva Deutschland GmbH

Contract Manufacturers · Feucht

Fareva Deutschland GmbH is a contract manufacturer based in Feucht, Germany.

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Fareva Deutschland GmbH – Address & Contact

Phone

Website

Address

Nürnberger Str. 12
90537 Feucht

Fareva Deutschland GmbH Overview

Fareva Deutschland GmbH is a contract manufacturer for pharmaceuticals or medical devices based in Feucht, Bavaria. The company produces on behalf of other companies and has a manufacturing license in accordance with Section 13 AMG.

Leistungen & Kapazitäten

Fareva Deutschland 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 Fareva Deutschland GmbH

Welcome to Fareva. Our 13,000 experts in industrial subcontracting are at your service. We support you in the household & industrial, beauty, makeup, pharmaceutical, and API sectors.

Location & Contact

Fareva Deutschland GmbH can be reached at the following address: Nürnberger Str. 12, 90537 Feucht – Phone: 091284040. 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 Fareva Deutschland GmbH produce pharmaceuticals, nutritional 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, Fareva Deutschland 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 Fareva Deutschland GmbH access to qualified specialists, a strong supplier industry and renowned pharmaceutical research institutions. The Feucht location enables short distances to clients and efficient logistics in the European internal market.

Frequently asked questions about Fareva Deutschland GmbH

What does Fareva Deutschland GmbH do?

Deutsche Tochter des französischen Lohnherstellers Fareva, spezialisiert auf Herstellung pharmazeutischer Spezialitäten.

Where is Fareva Deutschland GmbH located?

Fareva Deutschland GmbH hat seinen Sitz in Feucht. Detaillierte Kontaktdaten, Adresse und Telefonnummer finden Sie auf dieser Seite.

In which field does Fareva Deutschland GmbH operate?

Fareva Deutschland 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. Fareva Deutschland 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.

Fareva Deutschland GmbH on social media

Contract Manufacturers in Bayern

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

Last updated: 17.03.2026 · Category: Contract Manufacturers