B2B CONTRACT MFG

International Standard Cosmetics & Wellness Solutions

TOTAL QUALITY ASSURANCE

Zero-Compromise StandardsAnalytical
Testing

In cosmetics and personal care, trust is everything. TATVAM operates under uncompromising
WHO-GMP, ISO 22716, and US FDA standards. Every batch is certified with multi-stage
analytical testing, accelerated stability validation, and complete batch traceability.
WHO-GMP Compliant ISO 22716 & ISO 9001:2015 HPLC & Heavy Metal Assays 100% Clean & Cruelty-Free
RIGOROUS QC PHASES

Multi-Tier Quality Architecture for Complete Product Integrity

From raw ingredient quarantining to final container seal verification, our QA scientists follow documented standard operating procedures (SOPs).

We perform comprehensive organoleptic, physicochemical, and microbiological testing on every compounded batch. Stability chambers simulate accelerated 24-month climatic shelf life conditions (Zone IV-B) to verify zero phase separation, viscosity stability, and color retention.

Raw Material Quarantine & Assay: FTIR identification and HPLC purity checks before raw materials enter compounding halls.

Microbiological Bio-Burden Testing: Total aerobic microbial counts, yeast/mold screening, and pathogen absence confirmation.

Heavy Metal & Toxin Screening: Stringent ICP-MS checks ensuring zero detectable lead, arsenic, mercury, or cadmium.

Raw Material Analysis

Certificate of Analysis (COA) verification, botanical species authentication, and purity assays on all raw active ingredients and essential oils.

In-Process QC (IPQC)

Calibrated digital pH probes, Brookfield viscometers, refractometers, and specific gravity pycnometers test compounding stages continuously.

Accelerated Stability

Climatic test chambers simulate 40°C / 75% Relative Humidity for 90-180 days to validate minimum 24-36 months commercial shelf life.

Microbial Challenge (PET)

Preservative Efficacy Testing guarantees formulation safety against environmental spore contamination throughout consumer jar or bottle usage.

Packaging Compatibility

Vacuum chamber leak detection, cap torque testing, pump actuation volume checks, and label adhesion tests under humid transit conditions.

Batch Dossier & COA Release

Batch manufacturing record (BMR) sign-off by Qualified Persons (QP). Finished batch Certificate of Analysis released to client archives.

Our Compliance Standards

Manufactured in facilities audited and certified by internationally recognized accreditation bodies.

WHO-GMP

Good Mfg Practice

ISO 22716

Cosmetics GMP

ISO 9001:2015

Quality Mgmt

US FDA

Facility Registered

Cruelty-Free

100% Ethical

Halal Compliant

Clean Certified

Need Batch COAs or Sample Testing Reports?

Our regulatory and QA division will gladly share sample stability reports, microbiological limit assays, and documentation protocols for your brand review.

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