Standardised botanical extracts for dietary supplements
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Herbal Extract Supply for Supplement Brands

GMP-Certified Production · HPLC-Verified Assays · Batch Documentation
GMP & ISO Facilities · FSSAI · APEDA Verified

Standardised Botanical Extracts for Nutraceutical Manufacturing

SV Botanica provides certified, wholesale herbal extract supply designed specifically for supplement brands, contract development and manufacturing organisations (CDMOs), and private-label formulators globally. Sourced and processed in India under strict cGMP environments, our botanical portfolio covers over 60 active extracts engineered to meet the stringent physical, chemical, and microbiological thresholds required for solid dose encapsulation, tableting, effervescents, and liquid formulations.

HPLC-quantified active markers EU MRL & ETO contaminant testing Comprehensive batch QA dossiers
GMP FacilitiesISO CertifiedUSP / Ph. Eur. AssayedUSDA OrganicHalal AvailableKosher AvailableFSSAI Central LicenceAPEDA RegisteredHeavy Metals by ICP-MSFull Batch Traceability
Formulation Reliability

Engineered for Supplement Formulators

From clean-label demands to high-speed encapsulation, our active botanical extracts solve common production and compliance bottlenecks before raw materials arrive at your plant.

01

Marker Standardisation

Guaranteed active phytochemical percentages (withanolides, curcuminoids, bacosides, silymarin) verified by HPLC, UV, or titration methods defined clearly on each CoA.

02

Audit-Ready Dossiers

Complete documentation packages supplied as standard: complete batch CoA, Safety Data Sheets (SDS), technical specifications, allergen matrices, and non-GMO statements.

03

Physical Compatibility

Strict particle-size control (40 to 80 mesh) and consistent bulk density ensure superior flowability, minimal die-wall friction, and uniform blend distribution.

04

Regulatory Validation

Comprehensive third-party validation covering pesticide multiresidues (EU MRLs), ethylene oxide (ETO), irradiation screens, and ICP-MS elemental impurities.

Quality Infrastructure

Batch Analytical & Regulatory Deliverables

We do not treat documentation as an administrative afterthought. Every consignment is treated as an audited regulatory deliverable designed for seamless clearance through customs and QA quarantine.

Chromatographic Validation

Identity verification through TLC/HPTLC fingerprinting and quantitative assay analysis using calibrated HPLC instrumentation aligned to pharmacopoeial monographs.

Reference: USP / EP / BP Monographs

Contaminant & Safety Panels

Rigorous ICP-MS quantification for lead, arsenic, cadmium, and mercury, paired with complete microbiological screens (aerobic plate count, yeast & mold, Salmonella, E. coli).

Ref: Regulation (EU) 2023/915 · USP <2232>

Regulatory Dossier Pack

Every commercial lot arrives with a signed CoA, Technical Data Sheet, 16-section SDS, allergen statement, residual solvent screen (USP <467>), and non-irradiation certificate.

FSMA / FSVP Ready Documentation
Procurement Protocol

Export Execution in Four Predictable Steps

A rigorous supply protocol engineered around QA approval and specification alignment, ensuring complete transparency prior to bulk manufacturing.

01

Technical Brief

Submit your target monograph, active marker percentage, physical density, mesh requirement, and annual forecast.

Day 0
02

Specification Review

Our quality assurance desk provides a matching specification sheet, representative CoA, and firm freight pricing.

Within 24 Hours
03

Pre-Shipment Sample

We supply bench-scale validation samples with lot CoAs for laboratory verification and pilot formulation testing.

QC Sign-Off
04

Batch Release & Export

Final testing, release documentation, vacuum-sealed barrier packaging, and international freight dispatch.

On-Schedule Delivery
Knowledge & Technical Guidance

Insights for Nutraceutical Buyers

Analytical methodologies, international compliance protocols, and technical evaluations curated by our scientific regulatory desk.

Regulatory Protocol

EU Import Protocols for Indian Botanical Extracts

Comprehensive breakdown of official controls, ethylene oxide (ETO) testing requirements, and pesticide multiresidue monitoring under Regulation (EU) 2019/1793.

Procurement Guide

Ashwagandha Standardisation: Withanolides Sourcing

Technical evaluation of HPLC versus gravimetric testing, solvent selection risks, and plant-part authenticity in commercial Withania somnifera extracts.

Analytical Science

Curcumin 95%: Comparing HPLC and UV Assays

Why UV-Vis spectrophotometry overstates curcuminoid potency and how HPLC testing ensures accurate dosage compliance for brand integrity.

Purity Verification

Berberine HCl: Alkaloid Assay & Residual Solvents

Critical specifications for commercial Berberis aristata extracts, heavy metal controls, and addressing solvent screening parameters.

Procurement FAQs

Frequently Asked Questions

Direct answers concerning quality assurance, batch verification, and commercial shipping terms for dietary supplement brands.

We supply standardised active extracts including Ashwagandha, Turmeric Curcumin 95%, Boswellia Serrata, Berberine HCl, Brahmi (Bacopa monnieri), Milk Thistle, Lion's Mane, Rhodiola, and over 60 other botanical actives tailored for solid doses, capsules, and drink mixes.

All active phytochemical compounds (such as withanolides, curcuminoids, and boswellic acids) are quantified using validated HPLC, UV, or titration methods. The exact chromatographic assay method is documented explicitly on every lot Certificate of Analysis.

Every shipment comes complete with a Batch Certificate of Analysis (CoA), Technical Data Sheet (TDS), Safety Data Sheet (SDS/MSDS), ICP-MS heavy metals report, microbial profile, allergen statement, non-GMO declaration, and destination-specific phytosanitary certificates.

Standard MOQs typically start at 25 kg per ingredient in sealed, food-grade fibre drums. We also facilitate custom pilot-batch volumes and multi-metric-ton container loads for large contract manufacturers.

Yes. We dispatch pre-shipment samples accompanied by lot-specific Certificates of Analysis so R&D and QC departments can perform complete bench testing, flowability evaluations, and analytical verifications before release.

Technical Sourcing Support

Initiate Your Technical Sample & Quote Request

Connect with our technical exports desk for immediate assistance with active standardisations, analytical validation dossiers, and wholesale quotation terms.

Phone & WhatsApp Export Desk+91 8767675175
Commercial Inquiries[email protected]
Registered Global OperationsOffice No. 1044, Roongta Shopping Hub, Indira Nagar, Nashik, Maharashtra 422009, India

Request Ingredient Specifications & Commercial Pricing

Fast-track your procurement evaluation. Our regulatory and logistics teams provide technical data sheets, full batch CoAs, and pricing within one business day.

  • Confirmed botanical identification, plant part, and extraction method
  • Pre-shipment verification samples with matching analytical CoAs
  • Comprehensive batch QA dossiers: heavy metals, microbiology, and allergens
  • Direct manufacturer pricing with transparent CIF / FOB freight options
Get a Quote All enquiries are processed strictly under business-to-business confidentiality protocols.