3 Skin Sensitization Tests to Meet the EU Mandate

Mar 17th, 2017
Pascal Yvon, IDEA Tests Group, Martillac, France
ChemistryBeakerMolecule850

Editor’s note: This article is the seventh installment in a series covering the EU requirements for cosmetic products; see the previous: Part I, Part II, Part III, Part IV, Part V and Part VI.

Log in to view the full article
More in Regional
The #mydentity Guy Tang Reflect line of liquid demi permanent hair dyes is being recalled for potential contamination with nitrosamines.
Correction: Hair Products Recalled, Grande Cosmetics Settles and Sephora/Target 'Clean' Beauty Suits Continue
This roundup of products in "hot water" includes recalls on a hair dye and shampoo, Grande Cosmetics' settlement and a look at the latest "clean" beauty suits against Sephora and Target.
Jan 12th, 2024
Xforms is just one digital option available for creating an SPL file with cosmetic product facility registration and product listing information. Two additional electronic options are available.
FDA Debuts Digital SPL Xforms, Paper Forms for Cosmetics Facility, Product Submissions
The FDA has rolled out Structured Product Labeling (SPL) Xforms, a digital tool, and downloadable PDF forms to register cosmetic product facilities and list products, as mandated by MoCRA.
Jan 10th, 2024
Discover your skin’s mindfulness coach that improves your self-perception
Sponsored
Discover your skin’s mindfulness coach that improves your self-perception
Calisensix™ is an ingredient obtained from the bark of white willow and the stem cells from tomato. It resolves neurogenic inflammation, soothes discomfort and enhances pleasant sensations in sensitive skin, both self-perceived and objectively detected.
Apr 12th, 2024
Fda Computer Screen Adobe Stock 516632560 Editorial Use Only
FDA Opens Cosmetics Direct Registration Portal for MoCRA
Cosmetics Direct is an FDA Structured Product Labeling authoring tool that, according to the FDA, features user-friendly data entry forms.
Dec 18th, 2023
A responsible person is required to report serious adverse events associated with the use of cosmetic products in the U.S. to FDA within 15 business days.
FDA Releases Update to Ongoing Activities Related to Serious Adverse Event Reporting for MoCRA
A responsible person is required to report serious adverse events associated with the use of cosmetic products in the U.S. to FDA within 15 business days.
Dec 15th, 2023
According to the European Commission's Safety Gate, numerous products, ranging from soaps and fragrances, to body care, shampoo, bath milk and others, have been flagged for the present of the fragrance allergen butylphenyl methylpropional.
Recall Alert: L'Oreal's Mizani, J&J's Clean & Clear, Marcelle's 40+ Cream and Others
Globally, within the past couple of months, numerous cosmetic product recalls have been issued for microbe contamination and fragrance allergens, among other contaminants. Following is a roundup.
Dec 4th, 2023
'I think the biggest game-changer about [MoCRA's] ... requirement for GMPs is how it changes what it means to be adulterated,' Brandi Reinbold, senior manager of global certification for NSF International, said in this sponsored videocast. Register now to watch and learn more. It's free.
[video] GMP Standards to Meet MOCRA and Retailer Mandates of the Future
While the enforcement of MoCRA has been delayed until July 1, 2024, this is no time to rest on our laurels. As this sponsored video from NSF International explains, there's much to do and it will take time. Register now to watch and learn how to prepare.
Nov 27th, 2023
Beginning Dec.1, 2023, domestically produced toothpaste must be notified with the provincial-level drug supervision and administration department in the jurisdiction of the notification applicant before being marketed and sold.
China National Medical Products Administration Updates Toothpaste Regulations
Beginning Dec.1, 2023, domestically produced toothpaste must be notified with the provincial-level drug supervision and administration department in the jurisdiction of the notification applicant before being marketed and sold.
Nov 21st, 2023
The FDA does not intend to enforce the requirements related to cosmetic product facility registration and cosmetic product listing for an additional six months after the December 29, 2023, deadline.
FDA Delays MoCRA Enforcement by 6 Months
The U.S. Food and Drug Administration (FDA) announced it will delay the enforcement of facility registration and product listing requirements under MoCRA for six months after the Dec. 29, 2023, deadline to give the industry "sufficient time" to submit.
Nov 8th, 2023
While the concerns expressed over these materials are not specific to cosmetics, and only two are currently listed as cosmetic ingredients, it is worth noting the potential safety issues of these materials as well as the likelihood of the bans initiated in California to spread nationwide.
California Bans 4 Food Additives, FDA Proposes Same for BVO Emulsifier
On Oct. 7, 2023, the State of California banned four food and beverage additives reportedly linked to health issues: potassium bromate, propyl paraben, Red Dye No. 3 and brominated vegetable oil (BVO). The FDA may follow suit with BVO.
Nov 7th, 2023
October was the deadline but it came and went without a MOCRA portal to show for it.
FDA to Industry: Review SLP Guides, Gather Data Until MOCRA Portal Launches
October was the deadline but it came and went without a MOCRA portal to show for it. As the industry waits, the FDA advised members to continue collecting data and reviewing guidance documents — including the latest one for Structured Product Labeling.
Nov 3rd, 2023