-
E-MAIL
uscert@naver.com
-
E-MAIL
uscert@naver.com
-
TEL
02-529-8005
-
TEL
02-6226-9776
グローバルRA許認可
米国
What is VCRP (Voluntary Cosmetic Registration Program) as defined by the US (FDA)?
The VCRP is a voluntary system for reporting to the FDA by manufacturers, packers, and foreign manufacturers for export of cosmetic products for commercial distribution in the United States.
The VCRP program is divided into ‘manufacturer registration’ and ‘product ingredient registration’ for registration, and both submissions are encouraged, but you can choose whether to register or not by voluntary choice. (*VCRP is not a cosmetic approval program or promotional purpose, it was introduced to determine the safety of ingredients for cosmetics.)
• Advantages of VCRP
In order to register VCRP, cosmetics must consist of individual ingredients that have been proven safe by the FDA, and only products that have proven safety through cosmetic ingredient review (CIR) by the CIR expert panel can be registered. It can be seen that this has been proven.
• VCRP registration process
RCPE (Registration of Cosmetic Product Establishment)
VCRP manufacturing facility registration _ FDA2511 form confirmation
CPIS (Cosmetic Product Ingredients Statement)
Registration of cosmetic product ingredients and composition _ FDA2512
Peer review with FDA reviewers
What is RCPE (Registration of Cosmetic Product Establishment) as defined by the United States (FDA)?
Any cosmetic manufacturer intended for sale in the United States may register its establishment, either before or after commercial distribution of its products. If there is more than one production plant, the plant that handles the final production process must be registered. Information required for factory registration: company name, address, country of origin, position of the person in charge of FDA manufacturing factory registration, email address, and phone number After the registration application, FDA will assign a registration number to the applicant, and after registration is completed, the company list is published and managed on the FDA website. In the event of an accident that causes harm to human health or the death of an employee in the manufacturing plant, registration will be suspended, and if you do not report this to FDA within 10 days, your registration will be completely revoked.
•RCPE (VCRP facility registration)
Cosmetics manufacturer (Manufacturer)
Packer
Foreign manufacturer
• RCPE Checklist
Unable to register as a distributor
Submission of form for registration of facilities
In case of minor changes such as change of manufacturer's name, address, and product name after facility registration, submit a revised facility registration plan
What is CPIS (Product Ingredient and Composition Registration) as defined by the United States (FDA)?
Because VCRP is intended to enable purchasers in the United States to purchase its products, any cosmetic manufacturer that intends to sell in the United States must have a way to make their products available for purchase to consumers in the United States and then register the ingredients and composition of their products. (This applies to cosmetics currently sold in the United States.)
Information necessary for product ingredient and composition registration: brand name and cosmetic name, type of cosmetic, cosmetic ingredient, position in charge, email address, and phone number
After entering the cosmetic composition through VCRP, the CPIS registration number is granted by the FDA and activated
(*In case of including ingredients classified as drugs, registration and management are required in accordance with the Drug regulation)
When reporting, you must use the latest updated words from the International Cosmetic Ingredient Dictionary.
• Subject to CPIS (Product Ingredient and Composition Registration)
Cosmetics manufacturer (Manufacturer)
Packer
Distributor
Foreign manufacturer
• CPIS Checklist
Submission of form for product ingredient and composition registration
If the composition of the product is changed after registration of product ingredients and composition, submit amendments
(The FDA reassigns a CPIS number to each composition registered in the VCRP)