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Partnering

Two ways to use this plant.

Either bring a finished product and use the capacity, or bring a target profile and use the development. Most partners start with the first and move to the second once they have watched a few batches come off the line.

Licences
G/25/2431 · G/28/1774
Dosage forms
Tablets and capsules
Scales
Lab · pilot · commercial
Markets
ROW · ASEAN · domestic

Contract manufacturing

Capacity that flexes with the market, not against it.

The reason to manufacture through a third party is rarely price alone — it is that demand moves and an owned plant cannot. Contract manufacturing lets production scale up or down with the market, which is what makes it worth doing at all.

Site
GIDC Naroda, Ahmedabad, GujaratLicence numbers G/25/2431 and G/28/1774
Dosage forms
Solid oral — tablets and capsules
Annual capacity
1 billion general tablets and 220 million capsulesPlus 320 million effervescent tablets
Batch sizes
10 kg to 240 kg
Analytical support
Comprehensive, in-house, across the whole programme
Documentation
Dossier support for filings with the corresponding health and drug authorities

Areas of partnering interest

Where a conversation is most likely to go somewhere.

Beyond the general range, these are the four areas the plant is actively looking to partner in — because the equipment, the formulation experience and the existing registrations are all already pointed at them.

  1. 01

    Central nervous system

    Antidepressants, antiepileptics and neuropathic pain combinations, in tablets and capsules.

  2. 02

    Cardiovascular

    The largest developed range on the site: antihypertensives, statins, anticoagulants and antiplatelets, singly and in fixed-dose combination.

  3. 03

    Metabolic disorders

    Anti-diabetic single agents and combinations, including the prolonged-release metformin systems that most combinations are built on.

  4. 04

    Modified release

    Sustained, prolonged, delayed and enteric-coated presentations — the formulation work that separates a contract manufacturer from a packer.

How a programme runs

From an enquiry to a commercial batch.

Nothing unusual, but stated, so that a first conversation can be about the product rather than about the process.

  1. 01

    Brief

    A molecule or a target profile, a market to file in, a volume and a landed cost. Enough to say yes, no, or "not at that price".

  2. 02

    Feasibility

    Formulation and development assess the route, the excipient system and the release behaviour, and confirm what the plant can hold to.

  3. 03

    Development and scale-up

    Lab scale to pilot to commercial, with analytical method development and stability running alongside rather than afterwards.

  4. 04

    Documentation

    Dossier data for submission to the corresponding health and drug authorities, prepared for the market being filed in.

  5. 05

    Commercial supply

    Manufacture, in-process and finished-product testing, release, and packing in the blister format the market takes.

Enquiry

Four lines is a complete enquiry.

Molecule, market, volume, target price. Send those and the reply will be specific — including a straight no where the answer is no, which saves everybody a quarter.