Certificate of Analysis
Batch-specific COA is issued with every consignment and available on request for retained samples.
Request documentResources
Documentation & Downloads
Technical and regulatory documentation for our products, plus answers to the questions buyers ask most.
Safety Data Sheets
GHS-compliant MSDS in the format required for your destination market.
Request documentRegulatory dossiers
DMF and CEP support, along with TSE/BSE, nitrosamine and elemental impurity statements.
Request documentDownloadable certificates
WHO-GMP Certificate
Food & Drug Control Administration, Gujarat
ISO 9001:2015
Accredited certification body
GLP Certificate
National GLP Compliance Authority
FDA Registered Facility
US Food and Drug Administration
FAQ
Frequently Asked Questions
What is your minimum order quantity?
MOQ depends on the product — typically 1 kg for development quantities and 25 kg for commercial supply. Tell us your requirement and we will confirm.
Which pharmacopoeial standards do you supply to?
IP, BP, USP and EP grades are available for most products in our catalogue. Non-pharmacopoeial grades can be supplied against an agreed specification.
Do you provide samples?
Yes. Working samples with a batch COA are available to qualified buyers for evaluation and analytical method transfer.
What are your typical lead times?
Stocked items ship within 5–7 working days. Made-to-order campaigns typically run 3–5 weeks depending on the route and scale.
Can you support regulatory filings?
Yes. We support DMF and CEP filings and supply the associated open-part documentation, stability data and impurity profiles.
Privacy Policy
We collect only the details you submit through our inquiry form — name, contact details, company and your requirement — and use them solely to respond to your inquiry and maintain our commercial relationship. We do not sell or share this information with third parties. To have your details removed from our records, email info@harvinlabs.com.
Terms & Conditions
Product information on this site is provided for general guidance and does not constitute a binding offer. Specifications, availability and pricing are confirmed only in a written quotation. Products are supplied for pharmaceutical manufacturing use by appropriately licensed buyers, subject to the import and regulatory requirements of the destination country.