You will get Ongoing Regulatory Compliance Membership
Project details
Most compliance and formulation support comes from individuals who can build a product or a regulatory consultant who can review paperwork, rarely both in one person. My background bridges the two: formulation work across cosmetic and food manufacturing, plus regulatory compliance experience spanning US, EU, Canada, and CARICOM markets. That means a formula is reviewed for performance and shelf stability at the same time it is checked against the rules that determine whether it can actually be sold where a client intends to sell it, rather than catching a compliance gap after development is already finished.
Project Type
Business Consulting, Training & DevelopmentWhat's included $180
These options are included with the project scope.
$180
- Delivery Time 6 days
- Number of Revisions 1
Optional add-ons
You can add these on the next page.
Full Package Re-Review
(+ 4 Days)
+$60
Extra target market
(+ 3 Days)
+$30
Single Review Check
(+ 3 Days)
+$30About Tasannia
Cosmetic & Nutraceutical Formulator | GMP| US, EU,CAN,Caribbean
Kingston, Jamaica - 10:23 pm local time
You get a Scientist and Formulation Consultant with hands-on experience across cosmetics, personal care, food and nutraceuticals, translating your concept into ready formulations with the GMP-aligned documentation your contract manufacturer actually asks for: batch records, SOPs, and more that cut errors and speed up scale-up.
150+ formulations developed. 500+ GMP, HACCP, and ISO 9001:2015-compliant documents produced across US, EU, Canada and Caribbean markets.
What you get:
✔ Formulation development and reformulation, cosmetic and nutraceutical
✔ GMP-compliant SOPs, batch records, and technical documentation
✔ QC documentation,and product dossier
✔ Scale-up readiness review
Why brands stay:
✔ Deliverables that are structured, clear, and manufacturer-ready from day one
✔ Real-world regulatory and quality systems experience, not textbook advice
✔ Multi-market fluency across US, EU,Canada and Caribbean compliance requirements
If you're sitting on a formula idea, stuck on a manufacturer's QA requirements, or need documentation that actually passes review, send an invitation and let's get to work.
Steps for completing your project
After purchasing the project, send requirements so Tasannia can start the project.
Delivery time starts when Tasannia receives requirements from you.
Tasannia works on your project following the steps below.
Revisions may occur after the delivery date.
Step 1: Requirements review
I review the product concept, formula, or label you've shared, along with the target market and any specific concerns you've flagged.
Step 2: Formula, label, and documentation review
I assess the formulation for stability and safety risk, check label claims and ingredient declarations against your target market's rules, and flag any documentation gaps.