QUALITY & COMPLIANCE
Quality Is Built Into Every Stage
Quality at Micelle Innovative Labs is applied at ten control points across the product lifecycle, not just at finished-product inspection. Manufacturing procedures are cGMP-aligned, and every batch carries documentation from material receipt through release.
It begins with project review and continues through supplier qualification, material receipt, formulation, manufacturing, filling, packaging, documentation, testing, and release.
Our objective is to establish repeatable processes that protect product integrity and support consistent commercial production.
Quality Across the Product Lifecycle
- 01
Project Review
Requirements, formulation, and packaging are reviewed before work begins.
- 02
Supplier Qualification
Suppliers are evaluated against our material and documentation expectations.
- 03
Material Receipt
Incoming materials are checked against specification and receiving records.
- 04
Formulation
Formulas are prepared and documented under controlled instructions.
- 05
Manufacturing
Batches follow approved procedures with in-process checkpoints.
- 06
Filling
Fill operations are monitored for accuracy and container integrity.
- 07
Packaging
Labeling, coding, and packaging are verified against the approved specification.
- 08
Documentation
Batch records capture materials, process steps, and personnel.
- 09
Testing
Testing appropriate to the product category is coordinated as required.
- 10
Release
Records and finished-product requirements are reviewed before release.
Quality & Compliance Framework
These are the standards and registration frameworks our quality systems and manufacturing procedures are built around. They describe how we work — not a list of verified certificates.
- FDA registered
- NSF
- GMP
- USDA Organic
- UL GMP
- SQF
- ISO
- Kosher
- Halal
- OTC drug registration
Micelle Innovative Labs maintains quality systems and manufacturing procedures appropriate to the product categories produced within each division. Contact our team for current facility, registration, certification, testing, and product-scope information.
Continuous Improvement
Quality systems are reviewed on an ongoing basis. Process observations, deviations, client feedback, and production data are used to refine procedures, documentation, and training so that manufacturing stays predictable as volumes and product ranges grow.
Our commitment is to produce products intended to meet or exceed the regulatory and customer expectations that apply to each product category we manufacture.
Request Current Quality DocumentationRelated pages
Development and manufacturing capabilities
The phases a project moves through, from intake to commercial production.
About Micelle Innovative Labs
Founded in 2016 and operating two specialized laboratories in Carrollton, Texas.
Request current quality documentation
Ask our team for facility, registration, and testing information.
Ready to Build Your Product?
Tell us about your project and our team will respond within one business day.