GMP & AYUSH COMPLIANT AYURVEDIC CONTRACT MANUFACTURING
Divyaveda - Ancient Wisdom for Modern Wellness
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Quality Assurance

Analytical Standards & Regulatory Compliance

Ensuring formulation purity, botanical identity, and batch-to-batch consistency for domestic and global B2B supply.

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CERTIFIED B2B STANDARDS

Industrial Ayurvedic Integrity

Every formulation is validated against classical pharmacopoeial specifications, heavy metal thresholds, and full release testing documentation.

AYUSH Licensed • GMP Validated

Regulatory Compliance & Batch Documentation Framework

Production processes adhere strictly to statutory AYUSH drug manufacturing standards, in-process quality control benchmarks, and standardized analytical Certificate of Analysis (COA) release protocols.

Rigorous Governance

Three-Tier Quality Assurance Architecture

Every production batch undergoes strict quality gates at the raw material, in-process, and finished product release stages.

01

Raw Herb Authentication

Herbs and botanical inputs are screened for botanical species identity, organoleptic parameters, foreign matter, and initial moisture limits prior to warehouse acceptance.

02

In-Process Monitoring

Ongoing sampling during processing for blend homogeneity, tablet compression hardness, friability, disintegration time, and liquid viscosity.

03

Analytical Batch Release

Finished batches undergo analytical screening for heavy metals (Lead, Cadmium, Arsenic, Mercury), microbial limits, and active marker assays before release.

Analytical Verification

Standard Batch Certificate of Analysis (COA)

Every dispatched commercial lot is accompanied by a formal Certificate of Analysis detailing:

Physical ParametersDescription, color, odor, taste, average weight, disintegration time.
Chemical AnalysispH, total solids, refractive index, alcohol content (as applicable).
Heavy Metals AssayTesting for Pb, Cd, As, and Hg against pharmacopoeial safety thresholds.
Microbial CountTotal viable count, yeast & mold, absence of specified pathogens.
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