Quality & Safety
at Every Step
From thoughtful formulation and qualified ingredient sourcing to controlled manufacturing and finished-product testing, quality is ensured at every stage of the AIDEVI product journey.
Our Quality Standards
Four dimensions guide our evaluation of whether a product meets AIDEVI quality requirements.
Identity
Verify that raw materials and finished products contain the target ingredients listed on the label.
Purity
Evaluate purity and applicable impurity limits based on raw material and product specifications.
Strength & Composition
Verify that the key active ingredient content, formula composition, and serving size meet established specifications.
Safety Controls
Check microbial, heavy metal, pesticide residue, residual solvent, and other contaminant indicators based on product and raw material risk.
The FDA's dietary supplement cGMP framework requires companies to establish quality control, specifications, production records, and batch controls to ensure products meet established identity, purity, strength, and composition requirements.
Our Quality Process
A seven-step process from formula development to batch release, ensuring consistency and transparency at every stage.
Formula Development
Formula design and ingredient evaluation based on health goals and scientific research.
Supplier Qualification
Raw material supplier screening, document review, and qualification assessment.
Raw Material Verification
Verify identity, specifications, and quality of all incoming materials.
Pilot and Compatibility Review
Conduct small-scale pilot runs to evaluate mixing uniformity, dosage form compatibility, and process repeatability.
Controlled Manufacturing
Manufactured in compliance with dietary supplement cGMP standards.
Finished-Product Testing
Finished product testing for identity, purity, potency, and safety.
QA Review and Batch Release
The Quality Department reviews all records and test results before approving batch release.
Science-Driven Formulation
Every AIDEVI formula is engineered with purpose and precision. We don't just layer popular ingredients — each component plays a specific role in supporting your daily health goals.
Purpose-Driven Formulas
Each product is built around a clear daily health goal, avoiding the simple stacking of popular ingredients.
Ingredient Review
During formula development, we evaluate ingredient specifications, raw material quality, published research, ingredient compatibility, target dosage, dosage form suitability, and labeling requirements.
Dosage Form Development
Different dosage forms—capsules, tablets, gummies, powders, liquids, and sachets—require distinct development approaches to ensure optimal delivery and stability.
Pilot Runs
Before full-scale production, products undergo small-scale pilot runs to verify mixing uniformity, filling consistency, texture, liquid stability, packaging compatibility, and process repeatability.
Qualified Raw Materials
From supplier qualification to incoming material inspection, every raw material undergoes rigorous verification before production.
Supplier Qualification
- Supplier qualification audit
- Raw material specification review
- Supplier COA Review
- Raw material sourcing and origin verification
- Batch quality record review
- Supplier Quality Performance Evaluation
Incoming Material Review
Possible Test Categories
Testing requirements are selected based on ingredient type, product specifications, and applicable quality standards.
Controlled Manufacturing
"Controlled manufacturing" goes beyond facility registration. Here's what it entails at every level.
Manufacturing Standards
- Production in compliance with applicable dietary supplement cGMP requirements
- Written production procedures for each formula and batch size
- Batch production records for manufacturing, packaging, labeling, and storage
- Quality control across all production activities
Facility & Equipment Controls
- Production area hygiene management
- Employee training programs
- Equipment cleaning and calibration
- Prevent Cross-Contamination
- Material identification and segregation
- Environmental and storage condition monitoring
- Production line clearance procedures
In-Process Controls
- Raw material weight verification
- Mixing duration and sequence control
- Mixing uniformity checks
- Capsule fill weight, tablet weight, and hardness
- Packaging seal integrity
- Verify label and lot number
FDA 21 CFR Part 111 requires firms to establish and follow Current Good Manufacturing Practices to ensure dietary supplement quality and to ensure that actual packaging and labeling match production records. In-process controls vary by dosage form and are performed at defined manufacturing stages to support batch consistency.
Testing & Quality Assurance
Testing occurs at multiple stages — from raw materials to finished products — to ensure quality throughout the production process.
Raw Material Testing
Verifies that incoming raw materials meet specified requirements before production begins.
In-Process Testing
Confirms that key parameters and intermediate products meet specifications during manufacturing.
Finished-Product Testing
Confirms that final products meet release requirements, including identity, purity, potency, and safety criteria.
Testing Methods
Test methods are selected based on the ingredient, product specifications, and applicable market requirements.
QA Review and Batch Release
Completing testing does not automatically make a product ready for sale. The Quality team reviews all records before approving release.
- Supplier and raw material document review
- Batch production record review
- In-process control result review
- Finished product test result review
- Packaging and label verification
- Deviation and out-of-specification investigation
- QA final approval
- Nonconforming batch quarantine or disposition
Each completed batch is reviewed against defined specifications before release. Products that do not meet applicable requirements are held for investigation and appropriate disposition. cGMP requires batch production records and quality control procedures to ensure each production batch can be reviewed against established specifications.
Independent Third-Party Verification
In addition to internal quality reviews, selected AIDEVI products and batches undergo independent third-party testing for further verification.
Internal Quality Review
AIDEVI or the manufacturing quality team reviews raw material documentation, production records, in-process checks, and finished product results.
Independent Laboratory Verification
Selected products or batches are sent to independent third-party laboratories for applicable verification testing.
Selected AIDEVI products or batches undergo independent third-party testing. The applicable product, lot number, testing scope, and laboratory are specified in the corresponding report.
Batch Traceability & Certificate of Analysis
Every AIDEVI product has a unique lot number for full traceability. Find the lot number on the packaging to access quality documentation.
Batch Information
Quality Documents
COA displays analysis results for a specific sample. The SGS Report is issued by SGS for designated samples and test items. The GMP Certificate covers a specific manufacturing facility. The Certificate of Origin verifies the goods' source but does not confirm product efficacy or comprehensive safety.
Packaging, Stability, and Storage
Packaging Integrity
Stability and Shelf Life
- Storage conditions determined by stability studies
- Packaging Compatibility Assessment
- Temperature, humidity, and light requirements as specified on the label
- Shelf life varies by product due to formulation and dosage form.
Consumer Safety Guidance
Quality and safety go beyond production. Follow these key guidelines for safe supplement use.
The FDA also recommends that consumers read labels and consult doctors, pharmacists, or other healthcare professionals based on their personal medications and health conditions.
Frequently Asked Questions: Quality & Safety
AIDEVI's quality standards, testing procedures, and certifications.
Choose with Confidence
Seven-step quality process, independent verification, full-batch traceability — all for your peace of mind.
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