AROVELA
FOR PHARMACEUTICAL MANUFACTURERS

GMP-Grade Botanicals & Extracts for Pharma

USP/EP-grade plant material with ICH stability data and full batch genealogy for pharmaceutical and nutraceutical manufacturers.

Tired of botanicals that fail incoming QC?

Suppliers that can't deliver USP/EP pharmacopeia compliance lot after lot.

Heavy-metal and microbial limits that exceed your IPC release criteria.

Missing batch genealogy when auditors ask for field-to-API traceability.

Pharmacopeia-grade botanicals, audit-ready

USP/EP/JP compliance

Plant material released against USP, EP, JP and BP monographs — identity, assay and impurity testing per pharmacopeia.

ICH stability data

ICH Q1A long-term and accelerated stability studies on extracts, with retention samples held for 5 years.

Batch genealogy & traceability

Field GPS, harvest date, drying lot, extraction batch — every step linked by a single batch number from seed to drum.

Dedicated pharma-grade lines

Segregated pharma lines with HEPA-filtered drying, validated cleaning, and dedicated pharma-only QC release.

Audit-ready pharma supply

USP/EP
Pharmacopeia release
ICH Q1A
Stability data
5 yrs
Retention samples
100%
Batch traceability

Recommended SKUs for pharma

Standardized extracts and pharmacopeia-grade dried botanicals released for pharmaceutical use.

Certifications
ISO 9001GMPFDA RegisteredISO 22000

Pharma sourcing FAQ

Are your extracts USP/EP compliant?

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Yes. Our pharma-grade extracts are released against the relevant USP, EP, JP or BP monograph, with identity (TLC/HPLC), assay and impurity testing per pharmacopeia.

Do you provide heavy metals and microbial testing?

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Yes. Every pharma batch ships with heavy metals (Pb, Cd, Hg, As) per ICH Q3D and microbial limits per USP <61>/<62> and EP 2.6.12/2.6.13.

Can you support ICH stability programs?

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Yes. We run ICH Q1A long-term (25°C/60% RH) and accelerated (40°C/75% RH) stability studies on standardized extracts on request.

Do you maintain batch genealogy and DMF support?

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Yes. Every batch is traceable from field GPS through harvest, drying, extraction and packaging. We support DMF letters of authorization on contract.

Are your facilities GMP and FDA registered?

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Yes. We hold ISO 9001 and GMP certifications and are FDA registered for export to the United States.

Get a pharma-grade quote

Tell us your monograph and grade — we'll return COA samples and a price indication within 12 hours.

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