At All Season Herbs, quality assurance begins in the soil and does not end until the Certificate of Analysis is in your hands. Every step — from botanical sourcing to final packing — is governed by internationally recognised standards, independently verified, and fully documented.
This statement governs every decision we make — from which suppliers we qualify to which third-party labs we trust.
All Season Herbs is committed to providing the finest quality natural extracts and plant actives — consistently, traceably, and at the best possible value — to every client, in every market, without exception.
This is not an aspiration. It is an operating standard enforced at every level of our organisation. Our quality management systems are designed around the principles of Good Manufacturing Practice (GMP), Good Agricultural and Collection Practice (GACP), and WHO guidelines for herbal medicines.
Our founders come from a 70-year healthcare lineage — running hospitals and IVF centres where standards are a matter of lives, not just compliance. That same uncompromising standard governs every batch we manufacture.
We do not inspect quality into our products at the end. We build it in from the beginning — through a continuous, documented chain of controls spanning cultivation, sourcing, extraction, and final release.
GAP farming on our own 3,50,000 sq. ft. farm land. Dedicated supplier qualification with botanical identity checks before any raw material is approved.
Every supplier batch undergoes pre-shipment sample analysis — organoleptic testing, yield estimation, and assay — before authorisation.
On arrival, all raw materials are quarantined. A qualified QC officer extracts samples for immediate in-house testing before any material enters production.
Extraction yields, spray drying parameters, and blending uniformity are monitored at defined checkpoints with documented batch manufacturing records.
No product is released without a full Certificate of Analysis confirming identity, assay, microbial safety, heavy metals, pesticide residues, moisture, and particle size.
Our testing programme covers every parameter that matters to international pharmaceutical, nutraceutical, and food & beverage buyers — combining in-house instrumentation with NABL-accredited external laboratory partnerships.
Every raw material is botanically authenticated using organoleptic examination, microscopic analysis, and macroscopic characterisation to prevent adulteration and misidentification.
Active marker compounds are quantified to establish and verify standardisation levels — ensuring every batch carries the stated potency, verified against reference standards.
We test for residual solvents, heavy metal contamination (Pb, Cd, As, Hg), and pesticide residue levels through our NABL-accredited laboratory partners.
Total Aerobic Microbial Count, Yeast & Mould Count, and pathogen absence testing are performed on every batch, in line with USP, EP, and IP pharmacopoeial standards.
Physical characterisation ensures your product performs correctly in downstream formulation — including particle size distribution, bulk density, loss on drying, and pH.
Full Batch Manufacturing Records are maintained for every production run. Every shipment is accompanied by a Certificate of Analysis. Custom documentation can be arranged for regulatory requirements.
The herbal extract industry has long suffered from opacity. We are built differently. Our commitment to transparency is structural, not rhetorical.
Every document listed below can be provided to qualified buyers and regulatory teams.
Our certifications are not decorative. Each one represents a rigorous third-party audit — renewed on schedule and available for download.

Good Manufacturing Practice certification — the global benchmark for pharmaceutical and nutraceutical production quality and process control.
UK GMP · Current View Certificate ↗
ISO certification confirming our quality management systems meet globally recognised operational excellence standards.
ISO · Current Validity View Certificate ↗
Licensed by the Food Safety and Standards Authority of India — the central regulatory body governing food and food ingredient safety in India.
FSSAI · Renewed 2024–2026 View License ↗
Hazard Analysis and Critical Control Points certification — demonstrating systematic prevention of physical, chemical, and biological food safety hazards.
UK HACCP · Current View Certificate ↗
Halal certification enabling supply to Islamic markets globally — an essential requirement for GCC, Southeast Asian, and a growing number of EU markets.
Halal · Renewed 2024–2026 View Certificate ↗
Ministry of AYUSH export approval — formal government recognition of our compliance with India's traditional medicine and herbal product export standards.
Ministry of AYUSH · India View Certificate ↗
State FDA registration confirming compliance with Indian drug and food manufacturing regulations — a prerequisite for pharmaceutical-grade herbal extract supply.
FDA (India) · 2024 View Certificate ↗
Additional quality registration evidencing our compliance with export-facing regulatory requirements and our commitment to verifiable certification.
Current Validity View Certificate ↗We have formalised MOU-based relationships with internationally accredited laboratories — so when we provide a test result, it carries the authority of a name your regulatory team already knows.
One of the world's largest testing laboratory networks operating over 900 laboratories across 50+ countries. Our MOU with Eurofins enables internationally recognised test reports for heavy metals, pesticide residues, mycotoxins, and residual solvents.
A global leader in food safety and quality testing. Their reports are accepted by regulatory agencies across the US, EU, and Asia-Pacific markets.
Our in-house laboratory handles daily quality control — basic extractions, in-process monitoring, organoleptic evaluation, and preliminary assay work — enabling rapid decision-making without sacrificing rigour.
Traceability is the most critical — and most frequently missing — element in herbal supply chains. Our ownership of farm land, our dedicated supplier qualification programme, and our in-house processing from raw material to packing mean we can account for every stage of your product's journey.
We are one of the very few Indian herbal extract manufacturers who can demonstrate this level of supply chain control — and document it fully for your regulatory dossier.
Selected botanicals cultivated on our 3,50,000 sq. ft. GAP-certified farm lands adjoining the manufacturing facility.
Documented & Certified GAPAll external suppliers are formally qualified — audited against botanical identity, cultivation practices, and quality track record before onboarding.
Supplier Qualification RecordsPre-shipment samples are tested and formally approved before any order is placed. Rejected samples = rejected supply.
Tested & Approved Before OrderRaw materials are quarantined on arrival and retested in-house by our QC team before release into production.
Quarantine Records MaintainedEvery production batch carries a Batch Manufacturing Record. No product is released without a signed Certificate of Analysis.
Full BMR + CoA on ReleaseOur directors run hospitals and NABH-accredited IVF centres where sub-standard quality has direct patient consequences. We hold our herbal extracts to the same standard of accountability as a clinical product.
Most herbal extract manufacturers buy from open markets with no visibility into cultivation. We farm our own botanicals and formally qualify every external supplier — giving us raw material traceability very few Indian manufacturers can match.
GMP, ISO, FSSAI, HACCP, Halal, AYUSH Export, and FDA registration together enable us to supply pharmaceutical, nutraceutical, Ayurvedic, and food-grade clients globally — with documentation that satisfies local regulatory requirements.
We have nothing to hide — and everything to answer. Here are the questions our international clients ask most, and our honest answers.
Can I get a Certificate of Analysis before placing an order?
Yes, always. We provide a sample CoA for every product. For new clients, we are also happy to supply a reference sample with a full CoA so you can verify our quality claims independently before committing.
Are your products consistent batch to batch?
Yes — by design, not by chance. Our spray-dried extracts are blended in a 1,500-litre GMP SS blender to ensure absolute uniformity in colour, particle size, and active content across every batch.
Can I audit your facility?
Absolutely. We welcome client facility audits, supplier visits, and quality system reviews at any time. Our team will facilitate a thorough inspection and provide all documentation as needed.
Do your products meet EU / US Pharmacopoeia standards?
Yes, for applicable products. We test against USP, EP, IP, and WHO pharmacopoeial monographs as relevant. Our third-party lab reports from Eurofins and Mérieux NutriSciences are accepted by EU and US regulatory authorities.
Can you manufacture to custom specifications?
Yes. We offer contract manufacturing for custom extracts, spray-drying of client-supplied materials, custom blends, and bespoke standardisation levels — from R&D trials to commercial-scale production.
What is your minimum order quantity and lead time?
MOQ and lead times vary by product. We serve both large pharmaceutical manufacturers and smaller specialty formulators. Contact our team to discuss your specific volume and timeline requirements.
Are you truly Halal certified — covering the full production process?
Yes, our Halal certification covers our production facility and processes, not just the product. The most recent renewal is 2024–2026. We can provide the full certificate for your compliance records.
How do I know the botanical I'm ordering is authentic?
Every botanical is authenticated through macroscopic, microscopic, and organoleptic testing before entering production. Our CoA includes the botanical name, plant part used, country of origin, and extraction ratio. Adulteration has zero tolerance.
Request a Certificate of Analysis, a product sample, or arrange a facility audit. We are ready.