Quality & Safety
at Every Step
From thoughtful formulation and qualified ingredient sourcing to controlled manufacturing and finished-product testing, quality is considered throughout every stage of the AIDEVI product journey.
Our Quality Standards
Four dimensions guide how we evaluate whether a product meets AIDEVI quality requirements.
Identity
Confirm that raw materials and finished products contain the target ingredients declared on the label.
Purity
Evaluate purity and applicable impurity indicators based on raw material and product specifications.
Strength & Composition
Confirm key active ingredient content, formula composition, and serving size meet established specifications.
Safety Controls
Check applicable microbial, heavy metal, pesticide residue, residual solvent, or other contaminant indicators based on product and raw material risk.
FDA's dietary supplement cGMP framework requires firms 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 journey 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
Identity, specification, and quality confirmation for all incoming materials.
Pilot & Compatibility Review
Small-scale pilot runs to observe mixing uniformity, dosage form compatibility, and process repeatability.
Controlled Manufacturing
Production completed under defined conditions following dietary supplement cGMP requirements.
Finished-Product Testing
Applicable testing on finished products including identity, purity, potency, and safety indicators.
QA Review & Batch Release
Quality department reviews all records and test results before deciding on batch release.
Science-Led Formulation
Every AIDEVI formula is developed with purpose and precision. We don't simply stack popular ingredients — each component serves a clear role in supporting your daily health goals.
Purpose-Driven Formulas
Each product is designed around a clear daily health support goal, avoiding 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, sachets — adopt different development approaches to ensure optimal delivery and stability.
Pilot Runs
Before full-scale production, applicable products undergo small-scale pilot runs to observe mixing uniformity, filling consistency, texture, liquid stability, packaging compatibility, and process repeatability.
Qualified Raw Materials
From supplier qualification to incoming material review, every raw material goes through a rigorous verification process before entering production.
Supplier Qualification
- Supplier qualification audit
- Raw material specification review
- Supplier COA review
- Raw material source and origin confirmation
- Batch quality record review
- Supplier quality performance evaluation
Incoming Material Review
Possible Test Categories
Testing requirements are selected according to ingredient type, product specification and applicable quality requirements.
Controlled Manufacturing
"Controlled manufacturing" means more than just a facility registration. Here is what it involves at every level.
Manufacturing Standards
- Production following 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 implemented across all production activities
Facility & Equipment Controls
- Production area hygiene management
- Employee training programs
- Equipment cleaning and calibration
- Cross-contamination prevention
- Material identification and segregation
- Environmental and storage condition monitoring
- Production line clearance procedures
In-Process Controls
- Raw material weighing verification
- Mixing time and sequence control
- Mixing uniformity checks
- Capsule fill weight or tablet weight and hardness
- Packaging seal integrity
- Label and lot number verification
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 are consistent with 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 through finished products — to support quality at every point in the production journey.
Raw Material Testing
Confirms that incoming raw materials meet specified requirements before entering production.
In-Process Testing
Confirms that key parameters and intermediate products are within specification during manufacturing.
Finished-Product Testing
Confirms that final products meet release requirements including identity, purity, potency, and safety indicators.
Testing Methods
Test methods are selected based on the ingredient, product specification and applicable market requirements.
QA Review & Batch Release
Testing completion does not mean a product is automatically ready for sale. The quality department reviews all records before making a release decision.
- 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
- Non-conforming batch quarantine or disposition
Each finished 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 so that each production batch can be reviewed against established specifications.
Independent Third-Party Verification
In addition to internal quality review, selected AIDEVI products or batches undergo independent third-party testing for additional 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 identified in the corresponding report.
Batch Traceability & COA
Every AIDEVI product carries a unique lot number for full traceability. Find your lot number on the product packaging to access quality documentation.
Batch Information
Quality Documents
COA shows analysis results for a specific sample. SGS Report is issued by SGS for specified samples and test items. GMP Certificate covers a specific manufacturing facility. Certificate of Origin proves the source of goods but does not prove product efficacy or comprehensive safety.
Packaging, Stability & Storage
Packaging Integrity
Stability & Shelf Life
- Storage conditions determined through stability observations
- Packaging compatibility evaluation
- Temperature, humidity, and light requirements specified on label
- Different products may have different shelf lives based on formulation and dosage form
Consumer Safety Guidance
Quality and safety extend beyond production. Here are important guidelines for safe supplement use.
The FDA also recommends that consumers read labels and consult with doctors, pharmacists, or other healthcare professionals based on their personal medications and health conditions.
Common Questions About Quality & Safety
Everything you need to know about AIDEVI's quality standards, testing, and certifications.
Choose with Confidence
Seven-step quality process, independent verification, full batch traceability — all for your peace of mind.
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