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Learn what a Food Additive Petition (FAP) is, when FDA approval is required, and how to file it. Get expert help from Freyr Solutions. Start

Learn what a Food Additive Petition (FAP) is, when FDA approval is required, and how to file it. Get expert help from Freyr Solutions. Start your FAP today!

#FDA food additive petition #FAP submission requirements #FDA CFR regulations

Confused about EU BPR for disinfectants? Learn the full compliance process and get expert regulatory support from Freyr for smooth EU market

Confused about EU BPR for disinfectants? Learn the full compliance process and get expert regulatory support from Freyr for smooth EU market entry.

#Biocidal Product Regulations #EU BPR regulation #Biocidal product registration #BPR Compliance #disinfectant registration #Disinfectant market approval

Explore global regulations after the Red Dye No. 3 ban. Learn how food brands can ensure compliance and reformulate with natural colors. Con

Explore global regulations after the Red Dye No. 3 ban. Learn how food brands can ensure compliance and reformulate with natural colors. Contact us today!

#also known as Erythrosine #in foods and dietary supplements. This decision affects manufacturers all over the world.At the same time #this change is making the market for natural food colors grow quickly. It’s expected to reach over $3 billion by 2030. For people who handl #the challenge is replacing the banned dyes and dealing with the many rules about ingredients #how products are labeled #and getting approvals in different countries.The reason behind the ban on Red Dye No. 3 is mainly because of health concerns. Studies on an #and the U.S. National Toxicology Program classified it as a possible cancer-causing substance. On January 15 #2025 #the FDA made a final decision to stop using it in food and medicines that are taken by mouth. Companies have until January 15 #2027 #to change their food products and until January 18 #2028 #for medicines that are taken by mouth.Important things to remember from the regulatory side include:- All food and dietary supplement produ #which adds more pressure for food safety compliance.- Companies need to think about reformulating products globally #because similar concerns are happening in the EU #Canada #and other parts of Asia and the Pacific.Natural colors like beetroot extract #paprika #turmeric #and spirulina are becoming more popular as safer #clean-label alternatives to synthetic dyes. However #the rules for these natural ingredients vary a lot from one region to another.Key regulatory points for natural colors:- **USA**: FDA (CFR #and claims about natural origin must follow their labeling rules.Not following these rules can lead to product recalls #getting shipments rejected #or delays in entering new markets.When making changes to their products to follow the FDA ban on Red Dye No. 3 or to use natural colors #companies must follow strict regulatory steps:1. **Ingredient Replace Compliance**: Make sure the natural colors you choose are approved in #sensitivity to pH and light #and how much can be safely consumed daily.2. **Labeling and Claims Review**: Update your labels to show the new natural colors. Make sure a #like China #Brazil

Discover how top cosmetic brands use EU/UK regulations as a competitive edge. Learn how compliance drives growth. Consult Freyr’s experts to

Discover how top cosmetic brands use EU/UK regulations as a competitive edge. Learn how compliance drives growth. Consult Freyr’s experts today!

#EU cosmetics regulation #eu/uk cosmetics compliance #cosmetic regulatory compliance #UK cosmetic regulations #eu/uk cosmetics regulation #cosmetic regulations UK

Learn what NAFDAC is and how to register your cosmetic products in Nigeria. Ensure compliance with Freyr’s expert guide. Start your registra

Learn what NAFDAC is and how to register your cosmetic products in Nigeria. Ensure compliance with Freyr’s expert guide. Start your registration today!

#NAFDAC registration for cosmetics #NAFDAC registration #NAFDAC Nigeria #Nafdac Registration Certificate #NAFDAC registration requirements #NAFDAC approval

Australia’s cosmetic regulations with Freyr’s guide. Get expert support on AICIS registration, labeling, and compliance. Talk to us today

#Cosmetic Regulations Australia #AICIS Registration #Cosmetic Compliance Australia #australia cosmetic regulations #TGA Regulations #Cosmetic Labeling Requirements Australia

Launching in France? Get your FREE guide to DGCCRF compliance, food supplement labeling, registration & EU market entry in 2025. Download now!

Launching in France? Get your FREE guide to DGCCRF compliance, food supplement labeling, registration & EU market entry in 2025. Download no

#DGAL food notification #French food Regulatory authority

Freyr is a global Regulatory Solutions and services company offering services across the entire regulatory value-chain for Pharmaceuticals, Medical Devices, Biotech, Biosimilars, Consumer Healthcare companies across the globe.

#EU REACH Compliance Checklist #EU REACH Compliance

Freyr is a global Regulatory Solutions and services company offering services across the entire regulatory value-chain for Pharmaceuticals, Medical Devices, Biotech, Biosimilars, Consumer Healthcare companies across the globe.

#EU REACH Compliance Checklist #EU REACH Compliance

Need help with K-BPR or K-REACH in South Korea? Get expert guidance on biocidal product approval, documentation & regulatory compliance from

Need help with K-BPR or K-REACH in South Korea? Get expert guidance on biocidal product approval, documentation & regulatory compliance from Freyr.

#South Korea chemical registration #South Korea chemical regulations #Chemical compliance South Korea #Korean household product registration

Compare NDIN and GRAS Regulatory pathways with our clear infographic. Learn FDA requirements for food supplements & how to choose the correct route to compliance.

#FDA Regulatory pathways #Generally Recognized as Safe #New Dietary Ingredient Notification #FDA submission requirements

Stay CLP compliant with expert tips on hazard classification, labeling, SDS, & PCN. Ensure EU chemical safety with Freyr’s regulatory suppor

Stay CLP compliant with expert tips on hazard classification, labeling, SDS, PCN. Ensure EU chemical safety with Freyr’s regulatory support. Contact us now

#CLP regulation #CLP compliance #CLP labeling requirements #CLP hazard classification #CLP chemical labeling #EU CLP regulation #Classification Labelling Packaging #SDS compliance EU #Safety Data Sheet regulations EU #ECHA CLP notification #Poison Centre Notification (PCN)

Explore FDA's 2025 “healthy” claim rule & how it impacts food labeling. Get expert advice on reformulation, labeling updates, & FDA complian

Explore FDA 2025 “healthy” claim rule how it impacts food labeling. Get expert advice on reformulation, labeling updates, FDA compliance strategy

#FDA’s New Healthy Claims: Labeling Rules & Compliance Guide

Explore our PPWR infographic to meet 2025 packaging goals. Learn recyclability, EPR, labeling steps & act now to stay compliant. Download to

Explore our PPWR infographic to meet 2025 packaging goals. Learn recyclability, EPR, labeling steps & act now to stay compliant. Download today!

#PPWR #EU PPWR #Packaging and Packaging Waste Regulation #EU packaging regulation #EU packaging waste directive #Packaging waste regulation

Learn how to submit your CNF to Health Canada. Our infographic covers cosmetic product notification, labeling, & compliance for smooth marke

Learn how to submit your CNF to Health Canada. Our infographic covers cosmetic product notification, labeling, & compliance for smooth market entry in Canada.

#Health Canada cosmetic notification #Cosmetic Notification Form Canada #Cosmetic product registration #CNF Health Canada #Canada cosmetics regulations

Explore our essential ESG compliance checklist covering governance, risk, DEI, supply chain traceability, and reporting standards like CSRD, GRI & TCFD.

#ESG Compliance Checklist #ESG Compliance #ESG Reporting #ESG Strategy #ESG Framework #CSRD Compliance #Sustainability Compliance

REACH vs. TSCA: Comparing EU & US Chemical Regulations

Chemical regulations such as the EUS range and the US TSCA play an important role in ensuring the security of people and the environment. Both frameworks aim to manage chemical risks, but differ in their job, who they apply to, and what they have to do to comply with. Scope and reporting Rang (Chemical Registration, Evaluation, Approval, Restrictions) applies to all chemicals manufactured or imported in amounts of more than one tonne per year to the EU. It also covers finished products and mixtures of chemicals. The TSCA (Toxic Substance Control Act) applies to most industrial chemicals in the United States, except for products such as pesticides, foods, and drugs. In contrast to Reach, TSCA focuses more on new chemicals or new uses of existing substances. Registration requirements The registration process requires the company to register the substance before it can be sold by the European Chemical Agency (ECHA). Detailed technical documentation with certainty, use and risk is required. If it is not registered, it cannot be sold. This is "no data, no market management." According to TSCA requirements, businesses must submit a preparatory advertisement (PMN) to the U.S. Environmental Protection Agency (EPA) 90 days prior to the introduction of new chemicals. The EPA may assess risk, impose restrictions or deny approval. Chemical risk assessment and testing The company is responsible for certifying that the chemicals are safe. Hazard testing is stipulated based on public exchange of production volumes and key data. Special approval may be required due to high risk of carcinogenicity and persistent contaminants. In contrast, EPAs under TSCA assess risk. The updated TSCA Act requires that if the EPA represents an inappropriate risk, it must check and act on chemicals already in use. However, unless the EPA requires this, the tests are not automatically required. Substance restriction and enforcement Reach has several regulatory lists. List of candidates for highly problematic substances (SVHC) Approval List (Appendix XIV)Restrictions List (Appendix XVII) The TSCA has a central inventory of acceptable chemicals, which adds restrictions per case. There is no equivalent to achieving the approval process. Enforcement is also different. Reach is administered by the ECHA, but enforcement is handled by all EU member states. Therefore, ECHA registration is essential for businesses to sell their products in the EU. The TSCA is enforced by the EPA and can impose strong fines and penalties for violations. Suppliers and compatibility Reach compliance requires a safety data sheet (SDS), product identification, and a notification regarding poison centres. Non-EU companies must appoint a single representative (OD) to manage conformance. TSCA Compliance Compliance requires you to authenticate compliance, report usage, and keep a record for at least five years. Global Compliance Strategy Although both systems are intended for chemical security assessment, Reach is an industry operator and data-related, TSCA is governed by the government and focuses on EPA reviews. Companies working in both markets need to manage a variety of compliance strategies. Many choose to meet Reach's higher standards to simplify access to the global market. Freyr supports companies with reach and TSCA compliance, ensuring chemical registrations and regulatory permits are secured in both the EU and US markets.

#REACH vs TSCA #REACH Compliance #TSCA Compliance #TSCA requirements #chemical regulations #Chemical Safety Assessment #ECHA Registration

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