FDA cosmetic recall guidance: what brands should prepare for
FDA's final guidance explains when it can order a cosmetic recall and how brands can prepare their product and distribution records.
5 min read
Documentation
Who did what, and when? Reading a laboratory record
A measurement at 09:10, an entry at 09:25, and a review at 10:00 are different events. A laboratory record should make each understandable.
3 min read
Which formula did we make? Keeping versions identifiable
A pilot ticket says version 3, but its quantities match version 4. Here is how clear formula history helps resolve that mismatch.
3 min read
MoCRA safety substantiation: putting the product file together
A moisturiser example shows how product details, reports, and a qualified assessment fit together in a safety-substantiation file.
3 min read
A supplier changed an ingredient specification. What happens next?
A revised limit, test method, and material composition are different changes. Establish which occurred before accepting the next delivery.
3 min read
FDA cosmetics records access: reading the January 2026 draft
The January document is draft guidance on existing authority. Its status, scope, and passed comment deadline matter when reading the announcement.
1 min read
Taking a formula from the lab to production
A formula and a sample jar leave important gaps. Follow the information needed to take a laboratory lotion into a pilot batch.
2 min read
How to write a texture note someone else can use
Replace “luxurious” with a description of what happened in the jar, during spreading, and after application.
2 min read
How to make a batch record easier to follow
A worked example shows why “added more water, checked again, OK” is not enough for the next person reviewing a batch.
2 min read