Compliance Documentation
21 CFR Part 111 Supplement Manufacturing Documentation
PharmaVibes Research, a division of Stason Pharmaceuticals, manufactures food and dietary supplement products at a cGMP-compliant facility in Irvine, CA, in accordance with 21 CFR Part 111. We support 21 CFR Part 111 supplement manufacturing documentation, facility scope, partner credential scope, and quality records tied to the project.
Proof Scope
Compliance Documentation Scope
We keep public credential language scoped to approved claims and handle deeper documentation through qualified supplier review.
Irvine Facility Statement
PharmaVibes Research, a division of Stason Pharmaceuticals, manufactures food and dietary supplement products at a cGMP-compliant facility in Irvine, CA, in accordance with 21 CFR Part 111.
Quality Documentation
We support supplier review with project, quality, and manufacturing documentation aligned to the formula, format, and facility scope.
Partner Credential Scope
For selected partner-manufactured projects, we work with FDA-registered, GMP-certified manufacturing partners when that scope fits the product.
Supplier Review
We handle quality-documentation requests for procurement, regulatory, brand, and commercialization teams evaluating active projects.
Irvine Facility
cGMP-Compliant Irvine Manufacturing
PharmaVibes Research, a division of Stason Pharmaceuticals, manufactures food and dietary supplement products at a cGMP-compliant facility in Irvine, CA, in accordance with 21 CFR Part 111.
The Irvine facility anchors our supplier documentation support for food and dietary supplement projects. We keep facility language precise and separate it from partner-manufacturing claims.
Regulatory reference: 21 CFR Part 111 for dietary supplements.
Manufacturing Requirements
21 CFR Part 111 Supplement Manufacturing Scope
21 CFR Part 111 covers dietary supplement manufacturing, packaging, labeling, and holding operations. It defines current good manufacturing practice requirements for written procedures, personnel, production controls, quality control, packaging, labels, records, and complaint handling.
We use Part 111 language for the Irvine facility because it is the approved public scope. We do not convert compliance language into unverified certification claims.
Regulatory reference: 21 CFR Part 111 for dietary supplements.
Documentation
Quality Documentation Areas
Our documentation scope gives qualified teams direct supplier-review proof while keeping public claims tied to verified facility, partner, and project scope.
Facility and Entity Scope
We identify the relevant PharmaVibes Research, Stason Pharmaceuticals, Irvine facility, or selected partner-manufacturing scope for each project.
Formula and Format Records
We align formula status, dosage form, packaging direction, ingredient documentation, and finished-product requirements with the manufacturing program.
Quality Records
We support project-specific quality-record conversations where available documentation, confidentiality limits, and buyer review requirements are clear.
Partner Manufacturing Scope
For selected partner-manufactured projects, credential language stays tied to the applicable manufacturing partner and the product scope.
Request Scope
Quality Documentation for Supplier Review
We support quality-documentation requests for procurement, regulatory, and brand teams evaluating active supplement manufacturing projects.
- Irvine facility and entity scope for PharmaVibes Research and Stason Pharmaceuticals.
- 21 CFR Part 111 supplement manufacturing scope for food and dietary supplement projects.
- Project-specific formula, packaging, label, and finished-product documentation scope.
- Selected partner-manufacturing credential scope where partner manufacturing applies.
- Facility tour or technical review requests tied to qualified supplier evaluation.
Documentation details stay tied to verified facility, partner, and project scope for active manufacturing projects.
Related Capabilities
Manufacturing and Facility Proof
Facility media, controlled production areas, QA and laboratory views, equipment, packaging, and personnel proof.
Manufacturing Supplement Contract ManufacturingCapsules, tablets, powders, sachets, liquids, gels, packaging support, and selected partner manufacturing scope.
Formats Core Manufacturing CapabilitiesDosage-form breadth across capsule, tablet, powder, sachet, specialty format, packaging, and finished-goods work.
Company About PharmaVibes ResearchStason subsidiary relationship, Irvine-based team, product development model, and manufacturing support.
Supplier Review
Request Quality Documentation
We provide quality-documentation support for active supplement manufacturing projects, including facility scope, Part 111 scope, selected partner scope, and project documentation review.