Stefan Slezak Logistik Center Rheinland e.K.
Contract Manufacturers · Rheinbach
Stefan Slezak Logistik Center Rheinland e.K. is a contract manufacturer based in Rheinbach, Germany.
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Stefan Slezak Logistik Center Rheinland e.K. – Address & Contact
Stefan Slezak Logistik Center Rheinland e.K. Overview
Stefan Slezak Logistik Center Rheinland e.K. is a contract manufacturer for pharmaceuticals or medical devices based in Rheinbach, North Rhine-Westphalia. The company produces on behalf of other companies and has a manufacturing license in accordance with Section 13 AMG.
Leistungen & Kapazitäten
Stefan Slezak Logistik Center Rheinland e.K. 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
Stefan Slezak Logistik Center Rheinland e.K. can be reached at the following address: Industriestr. 7, 53359 Rheinbach – Phone: 02226911246. For current information and enquiries, please contact the company directly.
More information: Lohnhersteller in Nordrhein-Westfalen or all Lohnhersteller in Germany on Sanoliste.
Contract Manufacturing in der Pharmaindustrie
Contract manufacturing organizations (CMOs) like Stefan Slezak Logistik Center Rheinland e.K. produce medicines, 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
Stefan Slezak Logistik Center Rheinland e.K. As a contract manufacturer, 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 Nordrhein-Westfalen
North Rhine-Westphalia offers contract manufacturers such as Stefan Slezak Logistik Center Rheinland e.K. Access to qualified specialists, a strong supplier industry and renowned pharmaceutical research institutions. The Rheinbach location enables short distances to clients and efficient logistics in the European internal market.
Frequently asked questions about Stefan Slezak Logistik Center Rheinland e.K.
What does Stefan Slezak Logistik Center Rheinland do?
Das Logistik Center Rheinland ist ein Logistikdienstleister in Rheinbach. Das Unternehmen bietet E-Commerce-Fulfillment, Konfektionierung, Lettershop und Verlagsservice für Verlage und Online-Händler.
Was ist E-Commerce-Fulfillment?
E-Commerce-Fulfillment umfasst Lagerverwaltung, Auftragsabwicklung und Versand für Online-Händler. Das Logistik Center Rheinland übernimmt diese Prozesse komplett, damit Händler sich auf ihr Kerngeschäft konzentrieren können.
Where is das Logistik Center Rheinland based?
Stefan Slezak Logistik Center Rheinland e.K. hat seinen Sitz in Rheinbach bei Bonn, Nordrhein-Westfalen.
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. Stefan Slezak Logistik Center Rheinland e.K. 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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