ISO 9001:2015 (IMS)GMP CertifiedFSSAI LicensedAYUSH ApprovedIEC RegisteredU.S. FDA RegisteredISO 9001:2015 (IMS)GMP CertifiedFSSAI LicensedAYUSH ApprovedIEC RegisteredU.S. FDA Registered

Manufacturing

Eight production suites. One signed-off batch record per shift.

Our Hyderabad campus is engineered around a single principle — every dosage format on a dedicated line, every line tied to one quality system. The result: faster cycle time, cleaner traceability and a brief that doesn't get translated three times before it reaches the floor.

The lines

What runs on the floor today

Each suite is engineered for a specific format and stays that way — no shared product contact between solid-dose and semi-solid, no shared washdowns between liquids and personal care.

  • Bakery & Biscuits

    A dedicated rotary-moulder bakery with twin tunnel ovens and post-bake spray-dressing.

    Capacity
    Up to 8 metric tonnes per shift
    Outputs
    • Cookies
    • Crackers
    • Wafers
    • Functional bars
    • Rotary moulder + sheeter on the same line
    • Hot-air convection tunnel oven
    • Post-bake oil + sugar dressing
    • Pillow-pack and tray-flow wrapping
  • Dry & Wet Blending

    Parallel ribbon, conical and high-shear blenders feeding sachet, jar and pouch lines.

    Capacity
    Lots from 25 kg pilot to 2,000 kg commercial
    Outputs
    • Single-actives
    • Multi-component blends
    • Granules
    • Pre-mixes
    • Cleanroom-class blending hall
    • Online sieving & metal detection
    • Sachet, jar and pouch packing
    • Recipe lock + electronic batch records
  • Liquids & Syrups

    Steam-jacketed kettles, inline filtration and high-speed PET filling 100 ml – 1 L.

    Capacity
    Up to 24,000 bottles per shift
    Outputs
    • Juices
    • Tonics
    • Kashayams
    • Fortified syrups
    • Hot/cold filling with CIP washdown
    • Inline tunnel pasteuriser
    • Bottle rinser + air-knife dryer
    • Roll-on, screw-cap & ROPP capping
  • Tablets & Capsules

    Solid-dose suites with rotary presses, film-coater and auto-encapsulators.

    Capacity
    Up to 1.2 million tablets / 600,000 capsules per shift
    Outputs
    • Plain & coated tablets
    • Bi-layer tablets
    • HPMC vegan capsules
    • Gelatin capsules
    • Direct compression + wet granulation
    • Auto-coater, polish and inspection
    • Strip, blister and bottle packing
    • Tablet hardness & dissolution at line
  • Spreads, Gels & Creams

    Fully automatic semi-solid line with vacuum mixer, jacketed transfer and tube/jar fillers.

    Capacity
    Up to 3,000 jars / 6,000 tubes per shift
    Outputs
    • Nut butters
    • Functional spreads
    • Topical gels
    • Creams & lotions
    • Vacuum homogeniser to 30 µm
    • Hot/cold filling head
    • Tube cap-orient + induction seal
    • 100 % weight check + reject divert
  • Quality Lab

    Analytical, microbiology and stability suites — inline with production.

    Capacity
    Round-the-clock release testing
    Outputs
    • Raw-material release
    • In-process control
    • Finished-goods COA
    • Stability studies
    • HPLC, GC, GC-FID/ECD, UV-Vis
    • ICP-OES, AAS, KF titrators
    • Microbiology suite + LAF hoods
    • Stability chambers (25/40 °C, 60/75 % RH)

Capabilities

What you get when you contract with us

Reliability is engineered, not advertised. Four operational habits that customers feel in week three of working with us.

  • Multi-format under one roof

    Eight dosage formats live in eight engineered suites — so a single-vendor brief can run end-to-end here.

  • Recipe-to-pallet in 8 weeks

    Brief, prototype, scale-up, register, manufacture and ship — our default cycle for new private-label SKUs.

  • Documentation that holds up

    BMR, COA, stability, MSDS, allergen and audit dossiers ready before the first pallet leaves dispatch.

  • Clean operations

    Solar-augmented power, ETP discharge well within norms, and a returnable-packaging programme for B2B clients.

The process

Brief to bottle, in five clear stages

Each stage has a named owner, a documented hand-off, and a clear acceptance criterion before the next stage opens.

  1. 01

    Brief & feasibility

    Share the target product, claim and price point. We map it to a process, source-list the actives and confirm regulatory fit in one workshop.

  2. 02

    Formulation & pilot

    Our R&D team builds a stable prototype — taste / texture loops, organoleptic panels and an interim stability study before you sign off.

  3. 03

    Validation batch

    Pilot scales to a validation batch on the production suite. Three identical batches confirm process consistency and seed your stability programme.

  4. 04

    Commercial run

    Production runs on master batch records with electronic logs at every step. Each pallet ships with a finished-goods COA and traceable lot history.

  5. 05

    Stability & lifecycle

    We hold long-term and accelerated samples, refresh artwork on demand, and version-control your master formula for the lifetime of the SKU.

Want to see the lines in person?

Tours are arranged for serious buyers and registered customers — usually inside a week of asking. Bring your formula brief or visit just to see how the documentation system works in practice.

Schedule a tour