Our Quality
Uncompromising Standards.
Zero Hidden Fillers.
Every formulation. Every batch. Tested, verified, and certified to international pharmaceutical standards before it ever reaches you.
Potency
100%
Traceable
Our Quality Architecture ——
At Bodylia, quality is not a routine post-manufacturing inspection—it is the foundational architecture of every formula. From raw botanical harvesting to state-of-the-art cleanroom encapsulation, every step is rigorously governed by analytical chemistry and independent laboratory audits.
WHO-GMP Facility Governance
Formulated in automated cleanroom environments adhering strictly to World Health Organization Good Manufacturing Practices with zero human-touch contamination.
ICP-MS Heavy Metal Screening
Every batch undergoes Inductively Coupled Plasma Mass Spectrometry (ICP-MS) testing to verify lead, arsenic, cadmium, and mercury are well below USP safety thresholds.
NABL 3rd-Party Release
Independent NABL-accredited third-party laboratories test and validate finished products for potency, disintegration, bioburden, and stability prior to distribution.
100% Plant-Derived HPMC
Completely free from animal gelatins, bovine collagen, synthetic dyes, and titanium dioxide. Delivered exclusively in certified vegetarian plant-cellulose capsules.
The Three-Stage Quality Assurance Architecture
Every batch produced in audited WHO-GMP cleanrooms must successfully pass three independent testing milestones before it is cleared for release.
Identity & Purity Quarantine
Raw botanical extracts, chelated minerals, and bioactive vitamins undergo complete physical and chemical quarantine upon arrival at the facility.
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✓
HPLC & HPTLC Fingerprinting: Botanical identity and active marker verification.
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✓
ICP-MS Heavy Metals Assay: Screening for Lead, Arsenic, Cadmium, and Mercury.
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✓
Microbiological Bioburden: Absence of pathogenic yeast, molds, and bacteria.
Cleanroom Climate & Homogeneity
Automated climate controls protect light-sensitive and heat-sensitive cofactors, enzymes, and probiotics during processing and encapsulation.
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✓
Climate Regulation: Continuous monitoring maintaining <40% RH and <25°C temperature.
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✓
Dry Blending Uniformity: V-blender homogeneity assays ensuring uniform nutrient dispersion.
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✓
Automated In-Line Weight Checks: Strict capsule weight variation limit within <±3%.
Stability & Independent Release
Finished production batches are tested by independent NABL-accredited third-party laboratories to guarantee dissolution fidelity and stability.
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✓
In-Vitro Dissolution: Replicating gastric transit to guarantee release within 15–25 minutes.
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Accelerated Stability Testing: ICH guideline testing ensuring full potency over 36 months.
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✓
Batch Release Authorization: Signed Certificate of Analysis (CoA) issued per run.
Contaminant Limits & Analytical Benchmarks
We set internal release thresholds that are substantially stricter than statutory requirements. Below are the verified analytical testing parameters required for every Bodylia production batch:
| Test Parameter / Analyte | Bodylia Release Specification | Official Reference Standard | Testing Methodology | Batch Status |
|---|---|---|---|---|
| Lead (Pb) | < 0.5 ppm (mg/kg) | USP <2232> / FSSAI (Max 2.5 ppm) | ICP-MS (Inductively Coupled Plasma) | ✓ PASSED |
| Arsenic (As) | < 0.5 ppm (mg/kg) | USP <2232> (Max 1.5 ppm) | ICP-MS Spectrometry | ✓ PASSED |
| Cadmium (Cd) | < 0.3 ppm (mg/kg) | USP <2232> (Max 0.5 ppm) | ICP-MS Spectrometry | ✓ PASSED |
| Mercury (Hg) | < 0.1 ppm (mg/kg) | USP <2232> (Max 0.2 ppm) | ICP-MS Spectrometry | ✓ PASSED |
| Pesticide Residue Screen | Below Limit of Quantification (BLQ) | FSSAI Schedule IV & USP <561> | GC-MS / LC-MS-MS Screen (60+ analytes) | ✓ PASSED |
| Total Aerobic Microbial Count | < 1,000 CFU / gram | USP <2021> (Max 10,000 CFU/g) | NABL Microbial Culture Assay | ✓ PASSED |
| Yeast & Mold Count | < 100 CFU / gram | USP <2021> (Max 1,000 CFU/g) | Mycological Selective Agar | ✓ PASSED |
| Pathogens (Salmonella, E. coli, S. aureus) | Absent in 10 grams | USP <2022> / FSSAI Regulations | Selective Pathogen Enrichment Protocol | ✓ ABSENT |
| In-Vitro Capsule Disintegration | 15 to 25 minutes | USP <2040> Disintegration Benchmark | Simulated Gastric Fluid (37°C ± 1°C) | ✓ CONFORMS |
| Phytochemical Active Content | 100% of Label Claim (±5% tolerance) | Bodylia Monograph Specification | HPLC Reversed-Phase Chromatography | ✓ VERIFIED |
The Clean Label Standard
What we leave out of our supplements is just as crucial as what we put in. Bodylia adheres to strict clean-label architecture designed for optimal gastrointestinal tolerance and long-term health.
What Goes In
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✓
Standardized Botanical Extracts: Guaranteed active marker compounds (e.g. 5% Withanolides, 20% Shatavarins, 36mg PAC-A).
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✓
Bioavailable Active Nutrients: Methylcobalamin B12, Quatrefolic® active folate, Kaneka Ubiquinol®, and Liposomal iron.
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✓
100% Plant-Derived HPMC Shells: Natural pine-cellulose vegetable capsules with no animal collagen.
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✓
Photoprotective Packaging: Pure white UV-shielding recyclable bottles and nitrogen-sealed barrier pouches.
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✓
Full Quantitative Transparency: Exact milligram quantities declared for every ingredient—zero proprietary obfuscation.
What We NEVER Use
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✕
No Bovine Gelatin: Completely free from animal byproducts, porcine cartilage, and connective tissues.
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No Titanium Dioxide (TiO₂): Zero artificial whitening pigments or nano-particulate brighteners.
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No Artificial Colorants or Dyes: Free from FD&C Yellow, Red 40, and chemical opacifiers.
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No Hidden Proprietary Blends: We never hide low-cost bulk fillers behind deceptive "trade secret" matrixes.
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No Talc or Harmful Flow Agents: Only certified clean, pharmaceutical-grade excipients when strictly required for capsule flow.
Certifications You Can Trust
Our manufacturing operations and products are audited and certified by leading domestic and international regulatory authorities:
WHO-GMP Facility
Good Manufacturing Practices
ISO 22000:2018
Food Safety Management System
HACCP Certified
Hazard Analysis Critical Control Point
FSSAI Licensed
Lic. 10020043003314 & 10722999001018
100% Vegetarian
Plant-Derived HPMC ShellsRequest a Certificate of Analysis (CoA)
Every Bodylia bottle features a printed lot number and expiration date. We maintain complete analytical batch records and NABL third-party certificates for every production run.
Quality & Safety FAQs
Why does Bodylia use white HPMC capsules instead of clear or gelatin?
Pure white HPMC (hydroxypropyl methylcellulose) capsules protect light-sensitive micronutrients like active folates, CoQ10, and botanical flavonoids from photon degradation. Furthermore, HPMC is 100% vegetable-derived, dissolving smoothly without animal gelatin or digestive discomfort.
How do you verify heavy metal safety in botanical ingredients?
Every incoming raw botanical extract is subjected to Inductively Coupled Plasma Mass Spectrometry (ICP-MS) testing. This advanced analytical method detects trace elemental contaminants down to parts per billion (ppb), ensuring lead, cadmium, arsenic, and mercury remain far below USP limits.
Are Bodylia formulations tested on animals?
Never. Bodylia is committed to 100% ethical science. All safety, bioavailability, and clinical efficacy assessments are established through published peer-reviewed human clinical trials and in-vitro laboratory analysis.
What does ICMR DRI 2020 calibration mean for consumer safety?
Many imported supplements formulate with megadoses designed for North American adult males, which can place stress on renal and hepatic pathways. Bodylia calibrates its nutrient levels directly to the Indian Council of Medical Research (ICMR DRI 2020) benchmarks, ensuring optimum biological efficacy without risking nutrient toxicity.
