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Intas has invested heavily in
R & D and state-of-the-art manufacturing capabilities, in compliance with global standards and evolving formulations to meet the ever-growing demands of the competitive markets. Intas offers CRAMS Model (Contract Research and Manufacturing Services) to offshore clients from
regulated and semi-regulated markets.
The capability to develop new formulations, the technology transfer and contract manufacturing of established products at committed costs, quality and time creates the competitive advantage for
Intas. Moreover, the efficient and effective supply chain
management and a strong regulatory knowledge base make it one of the most sought after companies by global clients.
Intas extends excellent contract manufacturing support to more than 50 clients for around 150 products in regulated markets comprising Europe, Australia, New Zealand, USA and Canada.
The company has a significant share in Contract Research and Manufacturing
services in India and is making major headways with other global MNCs on this front. To fuel it further,
Intas has forged alliances with major pharma giants.
Intas boasts of
a state-of-the-art facility, duly approved by US FDA*,
UK MHRA, Australia TGA, South Africa MCC and WHO-GMP in Ahmedabad. The facility includes Solid Oral
manufacturing, Parenteral and Oncology Product
manufacturing with capabilities to produce dosage forms in sterile and general, covering
major therapeutic segments along with lyophilisation facility. The wide range of production techniques enables Intas to handle complex product packaging. There are two separate areas in Intas
manufacturing site isolated by "Barrier Isolation". One is general area having dedicated manufacturing facility for Effervescent, Narrow Therapeutics and Pellets. The second is a facility for Cytotoxic and Potent dosage forms.
Annual capacities for various dosage forms are:
| Dosage
Form |
Annual Capacity |
Regulatory Approvals |
| Oral Solids |
| Tablets & Capsules |
5.2 bn
Tab/Cap |
US
FDA*,
MHRA,
ANVISA, TGA, MCC |
| Effervescent
Tab |
50 Mn tablets |
GMP, WHO,
MHRA |
| Narrow
Therapeutics (Levothyroxin, Sodium, Warfarin Tablets etc.) |
900 Mn tablets |
GMP, WHO,
MHRA |
| Pellets |
30000 Kgs |
GMP, WHO,
MHRA |
| Injectables |
| Liquid
Ampoules |
85 Mn |
ANVISA, MCC |
| Liquid Vials |
30 Mn |
ANVISA, MCC |
| Lyophilised
Vials |
5 Mn |
ANVISA, MCC |
| Cytotoxic & Patent
Dosage Forms |
| Tablets & Capsules |
100 Mn |
US
FDA*,
MHRA, ANVISA, TGA, MCC |
| Liquid
Vials |
6.5 Mn |
US
FDA*,
MCC, TGA, ANVISA |
| Lyophilised Vial |
0.8 Mn |
US
FDA*,
MCC, TGA, ANVISA |
* Facility successfully inspected during December 2006. Approval awaited.
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