In July 2013, the European Union enforced a new set of regulations to replace the ec76/768. The purpose of the regulations is to govern the manufacturing, labeling and supply of cosmetic products. The new set of laws, unified the definition of cosmetics, labeling and ingredients which went a long way to abolish trade barriers among member countries in the Union. It also defined an EU cosmetics regulation responsible person to have legal obligations as the brand owner.
The new law defines a responsible person (RP) as who has an address in this Union and is legally bound to hold all the product documentation. The most important documentation the individual is responsible for the safety assessment in a Product Information File. The individual is required by law to maintain the document, compliance with EU legislation and have a comprehensive procedure for handling customer complaints.
The term responsible person is legal for an individual or group such as a company with certain pre-described obligation towards a product. It can be an individual agent in the European Union of the manufacturing company is based outside the European Union. Alternatively, the term may refer to the manufacturing company itself if based in the Union or one which orders the products manufacture. Also, the company involved in direct importation may play the role.
The role of a RP is very crucial especially for manufacturers not located within the Union. They make it possible to legally import goods as only those with a designated legal or natural individual can be imported. The law requires that the individual is identifiable in a precise and concise manner to legal obligations.
There are several obligations of the responsible individual under the law. For instance, they are required to notify the relevant authorities about products with undesirable effects to consumers. In addition, they should inform the CPNP about products being launched in the European market. A six month notification to the Commission is required if any of the products contain nano materials.
It is the role of the RP to ensure that goods entering into the market are safe and comply with regulations in the market. If a product represents a serious risk to human health, they should report it. In addition, they should comply with the competent authorities to solve the problem. Authorities also gather information from users and health officers. The particular government through the enforcing authorities is obliged to share such information with other member states in the EU.
Having an RP is beneficial to both the government and the business. For the business, it ensures that there is one single individual who acts as the contact point for any issues regarding regulation in the entire European Union. They help compile and update PIF promptly and accurately so that the goods reach the market faster. In addition, they ensure that products comply with the law so that the business is out of trouble.
The fact that there is one person to respond to crisis and questions makes it easier for the company to respond to emergency situations. Also, the government is able to trace one person compared to the whole company in case of emergencies. Even when importers change, the RP remains the same so that there is no need for re-notifications and reprinting of labels. Thus, the government saves time and money.
The new law defines a responsible person (RP) as who has an address in this Union and is legally bound to hold all the product documentation. The most important documentation the individual is responsible for the safety assessment in a Product Information File. The individual is required by law to maintain the document, compliance with EU legislation and have a comprehensive procedure for handling customer complaints.
The term responsible person is legal for an individual or group such as a company with certain pre-described obligation towards a product. It can be an individual agent in the European Union of the manufacturing company is based outside the European Union. Alternatively, the term may refer to the manufacturing company itself if based in the Union or one which orders the products manufacture. Also, the company involved in direct importation may play the role.
The role of a RP is very crucial especially for manufacturers not located within the Union. They make it possible to legally import goods as only those with a designated legal or natural individual can be imported. The law requires that the individual is identifiable in a precise and concise manner to legal obligations.
There are several obligations of the responsible individual under the law. For instance, they are required to notify the relevant authorities about products with undesirable effects to consumers. In addition, they should inform the CPNP about products being launched in the European market. A six month notification to the Commission is required if any of the products contain nano materials.
It is the role of the RP to ensure that goods entering into the market are safe and comply with regulations in the market. If a product represents a serious risk to human health, they should report it. In addition, they should comply with the competent authorities to solve the problem. Authorities also gather information from users and health officers. The particular government through the enforcing authorities is obliged to share such information with other member states in the EU.
Having an RP is beneficial to both the government and the business. For the business, it ensures that there is one single individual who acts as the contact point for any issues regarding regulation in the entire European Union. They help compile and update PIF promptly and accurately so that the goods reach the market faster. In addition, they ensure that products comply with the law so that the business is out of trouble.
The fact that there is one person to respond to crisis and questions makes it easier for the company to respond to emergency situations. Also, the government is able to trace one person compared to the whole company in case of emergencies. Even when importers change, the RP remains the same so that there is no need for re-notifications and reprinting of labels. Thus, the government saves time and money.
About the Author:
You can visit www.ceway.eu for more helpful information about Definition And Roles Of The EU Cosmetics Regulation Responsible Person.
No comments:
Post a Comment