Reporting suivant le California Safe Cosmetics Act

La règlementation californienne California Safe Cosmetics Act de 2005 requiert que certaines entreprises qui projettent de vendre leurs cosmétiques dans l’État de Californie reportent auprès du California Department of Public Health (CDPH) les ingrédients de leurs produits qui sont susceptibles de causer le cancer, des malformations congénitales ou d’autres troubles de la reproduction.

Au mois de juin 2017, plus de 900 ingrédients étaient soumis à reporting. Registrar Corp peut vous aider à déterminer quels sont les ingrédients de vos produits qui sont présents sur la liste de la Californie, et réaliser les reporting pour vous.

Complétez simplement le formulaire ci-dessous:

Please note that your information is saved on our server as you enter it.

This field is hidden when viewing the form
Send Incomplete
- sendIncomplete
This field is hidden when viewing the form
GCLID
This field is hidden when viewing the form
Landing Page
This field is hidden when viewing the form
International Office Email
This field is hidden when viewing the form
Form Type
This field is hidden when viewing the form
Download Type
This field is hidden when viewing the form
Inquiry Type*
This field is hidden when viewing the form
Industry
This field is hidden when viewing the form
Lead Source
This field is hidden when viewing the form
Lead Category
This field is hidden when viewing the form
Campaign Source
This field is hidden when viewing the form
Campaign Term
This field is hidden when viewing the form
Campaign Medium
This field is hidden when viewing the form
Campaign Name
This field is hidden when viewing the form
Campaign Content
This field is hidden when viewing the form
Match Type
My company imports*
- Seafood
- Juice
Detention Options
- I need assistance with a U.S. FDA Detention
- I need assistance with a U.S. FDA Import Alert
I would like to export to
I would like assistance with

Food and Beverages

Dietary Supplements

Medical Devices

Drugs

Cosmetics
This field is hidden when viewing the form
I would like assistance with
- Registration
- Agent Located in Region
- Labeling Requirements
- Good Manufacturing Practices
- Safety Plans
- Color Additives
- Adverse Event Reporting
- Master Files
- Other
Specify Other*
This field is hidden when viewing the form
Regulations Summary
What type(s) of Master File do you need assistance with?
What countries do you want to submit your Master File to?
Provide your company information
This field is hidden when viewing the form
Assessment Type
- Label Assessment
- Food Safety Plan Assessment
- Post BTA
This field is hidden when viewing the form
File to assess
- Food Safety Plan
- Product Labels
Is your Food Safety Plan FDA-Compliant?

U.S. FDA requires most types of registered food facilities to implement Hazard Analysis and Risk-Based Preventive Controls (HARPC) Plans. A HARPC plan must follow unique standards mandated by U.S. FDA. Other food safety systems may not completely satisfy FDA requirements.
U.S. FDA requires most types of registered food facilities to implement Hazard Analysis and Risk-Based Preventive Controls (HARPC) Plans. A HARPC plan must follow unique standards mandated by U.S. FDA. Other food safety systems may not completely satisfy FDA requirements.
Deadline Approaching for FDA's New Label Rules

Many food companies have less than 12 months to update their labeling to comply with new FDA labeling rules. The new rules include updates to the nutrition facts chart, serving sizes, mandatory declarations, and more.
Labeling mistakes result in more than 22% of all detentions in the United States.

Many companies do not realize their labels are non-compliant until their products are detained, which may result in delays, re-labeling expenses, or destruction of inventory. Help avoid costly issues in port. Have Registrar Corp's experts assess the FDA compliance of your labels.
Upload your current Food Safety Plan for a free assessment
Drop files here or

Max. file size: 50 MB.
Upload your product labels for a free preliminary assessment
Drop files here or

Max. file size: 50 MB.
Do you have your Registration and PIN?*
- Yes
- No
Do you have your FURLS Username and Password?*
- Yes
- No
NOTE: Registrar Corp cannot verify or recover your registration without:
- Your Registration Number and PIN
- or
- your FURLS Login and Password.
If you do not have either set of information, we encourage you to re-register.
Re-Register Now
Routing Number*
Country*
Company Name*
Contact Name*
Email*
Phone*
Physical Address*
City*
State / Province / Region
Postal Code
Is your company headquartered in the United States?*
Approximate Number of Suppliers
I Need Assistance With:
- Regulatory Updates via Email
- New FDA Food Facility Registration
- Renew FDA Food Facility Registration
- U.S. Agent Service for FDA Communications
- Facility 360
- FDA Prior Notice
- Labeling and Ingredient Review
- FCE-SID Regulations
- Preparing for FDA Inspection
- HACCP or HARPC Food Safety Plan
- Food Defense Plan
- Foreign Supplier Verification Program (FSVP)
- Detention/DWPE Assistance
- FDA Compliance Monitor
- Other
I Need Assistance With:
- Regulatory Updates via Email
- Drug Establishment Registration
- Drug Listings
- New Blanket No-Change Certification
- U.S. Agent and Registrant Contact
- Self-Identification for Generic Drugs
- Drug Labeling and Ingredient Requirements
- Drug Master Files
- eCTD Requirements
- Detention/DWPE Assistance
- FDA Compliance Monitor
- Other
I Need Assistance With:
- Regulatory Updates via Email
- Cosmetic Labeling and Ingredient Requirements
- California Safe Cosmetics Reporting
- Voluntary Cosmetic Registration Program (VCRP)
- Color Additives / Color Batch Certification
- Detention/Import Alert Assistance
- Other
I Need Assistance With:
- Regulatory Updates via Email
- Medical Device Establishment Registration
- U.S. Agent and/or Official Correspondent
- Device Listings
- Unique Device Identifier (UDI) Requirements
- Device Labeling Requirements
- Electronic Medical Device Reporting (eMDR)
- Medical Device Master Files (MAF)
- Detention/Import Alert Assistance
- Other
Specify Other*
Website
Comments
This field is hidden when viewing the form
Registration Status
FDA Registration Number*
(11 Digit Number)
FDA PIN*
(Please indicate capital letters)
FURLS Username*
FURLS Password*
Medical Device Owner / Operator Number
DUNS Number
Facility Establishment Identifier
Labeler Code
Compliance Information
FDA Registration Number
FDA PIN
List Products You Would Like to Ship*
Upload Labels for the Products Listed Above
Drop files here or

Max. file size: 50 MB.
Upload Food Safety Plan*
Drop files here or

Max. file size: 50 MB.
FCE Registration Number*
SID Numbers*
Upload Your Product Label
Max. file size: 15 MB.
Upload Your Food Safety Plan
Max. file size: 15 MB.
Upload Your Product Label
Drop files here or

Max. file size: 15 MB, Max. files: 10.
Upload Your Food Safety Plan
Drop files here or

Max. file size: 15 MB.
Upload Your HACCP Plan
Drop files here or

Max. file size: 15 MB.
Upload The Detention's Notice of Action
Drop files here or

Max. file size: 15 MB.
Upload your MMRs
Drop files here or

Max. file size: 15 MB.
I would like assistance with
- Export Listing Requirements
- Export Certificates
Which Products Would You Like Help With?
- Dairy Exports to Chile, China, or the EU
- Collagen and Gelatin Exports to the EU
- Seafood Exports to the EU or China
- Infant Formula Exports to China
What type of Export Certificate do you need?*
- Certificate to Foreign Government - Food
- Certificate of Free Sale - Dietary Supplements
- Certificate to Foreign Government - Medical Devices
- Certificate of a Pharmaceutical Product
- Certificate of a Cosmetic Product
- Health Certificates - Collagen and Gelatin Exported to the EU
Which best describes your device?*
- The manufacturer holds at least one NIOSHNIOSH uses very high standards to test and approve respirators for occupational uses. NIOSH-approved disposable respirators are marked with the manufacturer’s name, the part number (P/N), the protection provided by the filter (e.g., N-95), and "NIOSH," This information is printed on the facepiece, exhalation valve cover, or head straps. approval for a filtering facepiece respirator that is produced in accordance with applicable standards of authorization in other countries
- The device has a regulatory authorization under a jurisdiction other than China
- The device demonstrates acceptable performance to applicable standards documented by reports from a recognized independent test laboratory
- The device is on the Centers for Disease Control and Prevention (CDC) list of respirator alternatives during the COVID-19 pandemic.
NIOSH Approved Respirators*
Provide the following information for each of your NIOSH approved respirators
Manufacturer Name Model Number NIOSH Approval Number
Please provide the following information about your device
Manufacturer Name*
Manufacturer Address*
City*
State / Province / Region
Postal Code
Country*
Device Model Number*
How many respirators do you plan to send to the U.S.?
Upload your product label
Drop files here or

Max. file size: 50 MB.
Upload a marketing authorization document / certificate
Issued by another regulatory authority or conformity assessment body. Include the authorization number and name of the assessment body (if applicable)
Drop files here or

Max. file size: 50 MB.
Name of Testing Body
Upload Certificate of conformity to applicable standards
Drop files here or

Max. file size: 50 MB.
Upload test report
Report should demonstrate applicable performance standards have been met
Drop files here or

Max. file size: 50 MB.
CAPTCHA

Attention: les établissements pharmaceutiques et de dispositifs médicaux qui n’auront pas renouvelé leur enregistrement FDA en 2024 devront se réenregistrer.

Les établissements pharmaceutiques et de dispositifs médicaux enregistrés à la FDA doivent renouveler leurs enregistrements avant le 31 décembre 2025

Reporting suivant le California Safe Cosmetics Act

Reporting suivant le California Safe Cosmetics Act

Provide your company information

Is your Food Safety Plan FDA-Compliant?

Deadline Approaching for FDA's New Label Rules

Labeling mistakes result in more than 22% of all detentions in the United States.

Compliance Information

Contactez nous

Solutions

À propos

Rappel

Attention

Offre limitée

Afghanistan
Albania
Algeria
American Samoa
Andorra
Angola
Anguilla
Antarctica
Antigua and Barbuda
Argentina
Armenia
Aruba
Australia
Austria
Azerbaijan
Bahamas
Bahrain
Bangladesh
Barbados
Belarus
Belgium
Belize
Benin
Bermuda
Bhutan
Bolivia
Bonaire, Sint Eustatius and Saba
Bosnia and Herzegovina
Botswana
Bouvet Island
Brazil
British Indian Ocean Territory
Brunei Darrussalam
Bulgaria
Burkina Faso
Burundi
Cambodia
Cameroon
Canada
Cape Verde
Cayman Islands
Central African Republic
Chad
Chile
China
Christmas Island
Cocos Islands
Colombia
Comoros
Congo, Democratic Republic of the
Congo, Republic of the
Cook Islands
Costa Rica
Croatia
Cuba
Curaçao
Cyprus
Czech Republic
Côte d'Ivoire
Denmark
Djibouti
Dominica
Dominican Republic
Ecuador
Egypt
El Salvador
Equatorial Guinea
Eritrea
Estonia
Eswatini (Swaziland)
Ethiopia
Falkland Islands
Faroe Islands
Fiji
Finland
France
French Guiana
French Polynesia
French Southern Territories
Gabon
Gambia
Georgia
Germany
Ghana
Gibraltar
Greece
Greenland
Grenada
Guadeloupe
Guam
Guatemala
Guernsey
Guinea
Guinea-Bissau
Guyana
Haiti
Heard and McDonald Islands
Holy See
Honduras
Hong Kong
Hungary
Iceland
India
Indonesia
Iran
Iraq
Ireland
Isle of Man
Israel
Italy
Jamaica
Japan
Jersey
Jordan
Kazakhstan
Kenya
Kiribati
Kuwait
Kyrgyzstan
Lao People's Democratic Republic
Latvia
Lebanon
Lesotho
Liberia
Libya
Liechtenstein
Lithuania
Luxembourg
Macau
Macedonia
Madagascar
Malawi
Malaysia
Maldives
Mali
Malta
Marshall Islands
Martinique
Mauritania
Mauritius
Mayotte
Mexico
Micronesia
Moldova
Monaco
Mongolia
Montenegro
Montserrat
Morocco
Mozambique
Myanmar
Namibia
Nauru
Nepal
Netherlands
New Caledonia
New Zealand
Nicaragua
Niger
Nigeria
Niue
Norfolk Island
North Korea
Northern Mariana Islands
Norway
Oman
Pakistan
Palau
Palestine, State of
Panama
Papua New Guinea
Paraguay
Peru
Philippines
Pitcairn
Poland
Portugal
Puerto Rico
Qatar
Romania
Russia
Rwanda
Réunion
Saint Barthélemy
Saint Helena
Saint Kitts and Nevis
Saint Lucia
Saint Martin
Saint Pierre and Miquelon
Saint Vincent and the Grenadines
Samoa
San Marino
Sao Tome and Principe
Saudi Arabia
Senegal
Serbia
Seychelles
Sierra Leone
Singapore
Sint Maarten
Slovakia
Slovenia
Solomon Islands
Somalia
South Africa
South Georgia
South Korea
South Sudan
Spain
Sri Lanka
Sudan
Suriname
Svalbard and Jan Mayen Islands
Sweden
Switzerland
Syria
Taiwan
Tajikistan
Tanzania
Thailand
Timor-Leste
Togo
Tokelau
Tonga
Trinidad and Tobago
Tunisia
Turkey
Turkmenistan
Turks and Caicos Islands
Tuvalu
US Minor Outlying Islands
Uganda
Ukraine
United Arab Emirates
United Kingdom
United States
Uruguay
Uzbekistan
Vanuatu
Venezuela
Vietnam
Virgin Islands, British
Virgin Islands, U.S.
Wallis and Futuna
Western Sahara
Yemen
Zambia
Zimbabwe
Åland Islands

Manufacturer Name	Model Number	NIOSH Approval Number