AashishFormulations

Commercial models

Domestic supply and international export.

Engagement models for formulation manufacturers, capsule filling plants and distributors.

India

Domestic pharmaceutical supply

Finished-dosage manufacturers, capsule formulators and secondary pellet processors across India’s pharmaceutical clusters.

From neutral sugar spheres made on the dedicated first floor to gastro-resistant enteric pellets, domestic supply is built around short transit and batch consistency.

  • Direct supply from the Hyderabad campus.
  • Batch sizes from 200 kg through multi-ton contracts.
  • Certificates of analysis against IP, BP and USP monographs.

Export

International business

An active Import Export Code and proximity to Hyderabad airport and dry-port terminals support overseas buyers, with export-grade packaging.

International work is qualified against the destination regulatory dossier, product registration and climatic-zone stability, including Zone IV A and Zone IV B.

  • Active IEC for cross-border shipment.
  • Open Part DMF packages in preparation — not yet filed as accepted DMFs.
  • Export drums with dual hermetic liners.

Workflow

Twelve steps from enquiry to dispatch.

  1. 01

    Business enquiry

    Received through the technical portal, direct business-development contact, or a referral.

  2. 02

    Buyer qualification

    Corporate identity, destination country and drug application are verified.

  3. 03

    Specification review

    Drug load (% w/w), pharmacopoeia (IP/USP/BP) and volume are confirmed.

  4. 04

    QA / RA review

    Documentation needs, monograph alignment and test parameters are reviewed.

  5. 05

    Sample evaluation

    Technical samples and a certificate of analysis are sent for laboratory fill trials.

  6. 06

    Commercial quotation

    Pricing, delivery, release terms and Incoterms.

  7. 07

    Approval and purchase order

    Specifications are approved, supply terms are executed, and a purchase order is issued.

  8. 08

    Manufacturing

    The batch is staged in a 200 kg, 300 kg or 500 kg fluid bed suite.

  9. 09

    QC release testing

    Assay by HPLC, dissolution on eight bowls, moisture by Karl Fischer, and particle size.

  10. 10

    QA batch release

    Batch manufacturing record audit, certificate of analysis and formal release.

  11. 11

    Packaging

    Double heat-sealed polyethylene liners with desiccant, inside tamper-evident HDPE containers.

  12. 12

    Dispatch

    Climate-controlled domestic transport, or export staging with the dossier packet.

Start a sourcing discussion.

Specifications, lead times and confidential sample protocols, with the business development team.