REGULATORY SUPPORT & REGISTRATION

Food supplement regulatory and registration support.

We jointly plan product category, ingredient, label and technical file requirements from the start of development.

SERVICE SCOPE

We plan your product alongside its regulatory requirements.

Product category, ingredient structure, label claims and required files are assessed within the relevant regulatory framework; your project team receives support with registration and notification processes.

REGULATORY SUPPORT & REGISTRATION service
REGULATORY SUPPORT & REGISTRATIONCategory · Label · Technical file · Follow-up
WHAT DOES IT INCLUDE?
  • Product category and regulatory checks
  • Label copy and mandatory statement review
  • Technical file preparation support
  • Registration and notification coordination
PROJECT DELIVERABLES
  • 01Regulatory checklist
  • 02Label compliance assessment
  • 03Required document list
  • 04Application process roadmap
HOW WE WORK

Controlled progress in three steps.

01ReviewProduct ingredients and category are assessed.
02PreparationLabel and technical file requirements are completed.
03Follow-upRegistration or notification steps are coordinated.
REGULATORY-COMPLIANT PRODUCT DEVELOPMENT

Regulatory support for food supplements and cosmetics

Product category, ingredients, label text and presentation to market should be considered together from the start of development. Early regulatory assessment reduces extensive late-stage revisions to the formula or packaging.

Ingredient and label compliance

Ingredients, usage quantities, mandatory information and product claims in food supplement and cosmetics projects are assessed against the relevant requirements. Labels and carton copy are technically checked before designs go to print.

Registration, notification and technical file preparation

Documents and information required for the product are planned with the project team. Consistently prepared technical documents, formula information and packaging copy support registration or notification.

FREQUENTLY ASKED QUESTIONS

Answers to key questions.

When should regulatory checks begin?

They should start when ingredients and product category are defined, allowing formula, label and packaging revisions to be planned before manufacturing.

Is label copy also checked?

Yes. Mandatory information, directions for use, the ingredient list and product claims are assessed within the relevant product category’s requirements.

How long do registration and notification take?

Timing may vary with the product category, file scope and relevant processes. A project-specific roadmap is prepared once the required documents are identified.

MANUFACTURING GUIDE

Regulatory compliance in product development

Ingredients, claims, labeling and notification for food supplements and cosmetics are addressed according to the target market’s requirements. Early regulatory assessment reduces project losses.

Checking formulas and packaging copy before production supports smoother registration, notification and market launch processes.

MANUFACTURE WITH İNOVENTİS

Let’s bring your idea into production together.

Let’s create a production roadmap tailored to your project, from formulation to packaging.

Let’s discuss your project