Quality
Built for inspection.
A pharmaceutical quality system is applied to every product we make. We write rigorous SOPs, review every Batch Manufacturing Record (BMR), and our QA/QC unit makes every release decision.
The system
One quality system for every product, whether it carries a partner’s label or our own.
Seven-10 operates a GMP-certified manufacturing facility in Montego Bay, Jamaica. Nutraceuticals and functional nutrition products are manufactured under the same procedures, documentation and release controls used for pharmaceutical products: qualified materials, validated processes, trained personnel and a complete record for every batch. The system is built to withstand inspection by regulators, importers and brand partners in every market we serve.
MaterialsIncoming materials are received against documented specifications, from qualified suppliers, with identity confirmed before use.
ProcessManufacturing follows approved batch instructions with in-process checks and full traceability from raw material to finished lot.
TestingCertificates of Analysis are issued on testing by ISO 17025 accredited laboratories.
ReleaseEvery commercial batch is released on documented evidence, with a Certificate of Analysis (COA) and a complete, QA/QC-reviewed BMR retained on file.
Regulatory and export
Documentation that travels with the product.
Our products are manufactured for export. Regulated markets require thorough documentation across multiple categories for products containing active compounds, from specifications and batch records to certificates of analysis, stability data and the licences and certificates that stand behind the facility. We prepare that documentation as part of every programme, so that import and export operations proceed without interruption. Brazil is a primary focus market, and our documentation is prepared with that regulatory environment in mind. It follows the product to the partner, the importer and the regulator through the proper channels.
Specifications
Written for every raw material and finished product, and kept under change control.
Certificates of Analysis
Third-party ISO-17025 accredited labs validate commercial batches.
Batch Manufacturing Records
Complete, reviewed and retained, so any lot can be reconstructed from receipt of materials to release.
Country-of-origin support
Facility credentials, product dossiers and partner brand pages that regulators can review directly.
Documentation for partner products is available for the importers and regulators who require it. Partners with an active manufacturing and supply programme can log in to access their product documentation in the Partner Portal.