ケーススタディ

Safe Pharmaceutical Products with Sealing

ケーススタディ

At Krewel Meuselbach GmbH

The medium-sized pharmaceuticals company Krewel Meuselbach GmbH manufactures top-quality, affordable pharmaceuticals at its Eitorf (North Rhine-Westphalia) and Gehren (Thuringia) sites in Germany, using state-of-the art technology. The pharmaceuticals specialist has been putting its trust in METTLER TOLEDO solutions for a number of years now.

Traceability and Prevention of Product Falsification

At the Eitorf site, Krewel Meuselbach uses the compact XS2 MV TE system from METTLER TOLEDO in a thermoforming line to ensure comprehensive quality control and prevent the falsification of its products. It achieves this through data matrix codes and tamper-evident seals.

The XS2 MV TE combines precise weighing, marking, sealing, and verification with global requirements for traceability and the prevention of product falsification – even meeting the market requirements of the future. This is especially important for a pharmaceuticals manufacturer like Krewel Meuselbach, which produces goods in line with EU Directive 2011/62/EU and the GMP standard, and markets its products on an international level.

XS2 MV TE

“The XS2 MV TE system has proven to be a reliable solution that meets our requirements when it comes to safety markings and tamper-evident seals. What’s more, it integrates perfectly into our existing production environments in Eitorf and Gehren,” explains Hilmar Höhne, Head of the Technical Department at Krewel Meuselbach.

4-in-1 System Combines Checkweighing, Serialization, Opticalcode Verification and Tamper-evident Seal applicator in one Reliable Unit

The spacesaving combination system XS2 MV TE offers reliable checkweighing with serialization, optical code verification and a tamper-evident seal applicator. The weighing unit ensures the completeness of the pharmaceutical packaging. If, for example, the contents are missing or a blister is incomplete, the product is automatically removed from the production line by means of an air jet.

Related White Papers

Validation, Verification and Monitoring For Product Inspection Equipment
このホワイトペーパーでは、インライン製品検査装置のバリデーション、ベリフィケーション、および日常的なパフォーマンスモニタリングの必須プロセスに関するガイダンスを提供しています。
FSMA最終要件
新しい食品安全強化法(FSMA)について、また施設を準備する方法について詳細をご説明しています。
HACCP Versus HARPC- What is the Difference?
このホワイトペーパーでは、HACCPとHARPCの共通点と相違点を説明しています。
最適の状態に調整された充填プロセス– PDFの無料ダウンロード
充填プロセスを制御することは、近年の生産ラインが直面している最も重要な課題の一つであり、品質や採算性、顧客満足に直接影響を与えます。