Advantages of Machine Vision Inspection
Implementing a machine vision inspection program brings advantages to the production process, including increased brand protection and improved efficiency.
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In order to ensure the safety of consumers, labeling regulations are in place for cosmetic products mandating the presence of information required by governing bodies. In some countries, failure to adhere to the regulations may result in an outright ban on the sale of that product in the region.
While many countries are working together to develop regulations that are aligned, significant differences in regional requirements still remain.
This white paper seeks to outline regulations governing the labeling of cosmetics in key global regions. It provides useful guidance for manufacturers already trading in these markets as well as those looking to enter.
The white paper focuses on the regulations in three major economic regions:
- United States
- European Union
- China
Download this informative white paper to learn more
In the highly competitive cosmetics market, it is more important than ever for manufacturers to do everything necessary to make their products stand out to the average consumer. Accomplishing this goal often relies on making product labels which will catch the eye of potential consumers and effectively make an argument for the product. When designing those new labels, however, it is important to keep the legal requirements of the intended market in mind.
In recent years the United States and European Union have both attempted to unify their regulations in an effort to make trade between territories easier. However there are still some significant differences between the two regions mostly relating to local terms used for particular ingredients. Unfortunately this means that no label design exists which would satisfy every requirement. Manufacturers must therefore continue to rely on multiple label designs in order to sell into different territories, which means keeping up to date with the latest regulations
Related White Papers
米国、EU、中国における医療機器のラベリングに関する主要な要件をまとめたホワイトペーパーです。
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。
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。
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。
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