Improving access to quality medicines

Biosimilar Production Capabilities

CuraTeQ’s end-to-end biosimilar production facility is a fully equipped 40,000 sq. ft. commercial scale manufacturing and R&D centre, with dedicated laboratories to support all biosimilar research and development, production and quality control activities.

 

Biosimilar production requires a strong research and development footprint and expert scientific resources. Our production centre in Hyderabad, India has end-to-end capabilities for producing a full range of products from bulk drug substance (DS) to fill-finish and packaged drug products (DP).

 

The Quality Control Laboratories at our production centre are engaged in all physicochemical, analytical and microbiological analyses involved in the verification and testing of biological products and are instrumental in undertaking method transfer, compendial method verification and method validation activities. Biosimilar research and development requires a strong research and development footprint and expert scientific resources.

What are Biosimilars?

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Biosimilar Production 2

Biosimilar Research and Development

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Biosimilar Production 3

Biosimilar Manufacturing Capabilities

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Biosimilar Production 4

Quality Control Laboratories

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Latest News

CuraTeQ Biologics receives UK MHRA approval for Bevqolva™ (Bevacizumab biosimilar)
Press Release

21 December 24

CuraTeQ Biologics receives UK MHRA approval for Bevqolva™ (Bevacizumab biosimilar)

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CuraTeQ Biologics receives CHMP positive opinion for Filgrastim biosimilar
Press Release

13 December 24

CuraTeQ Biologics receives CHMP positive opinion for Filgrastim biosimilar

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EMA grants GMP certificate to CuraTeQ Biologics’ manufacturing facility in Hyderabad
Press Release

12 November 24

EMA grants GMP certificate to CuraTeQ Biologics’ manufacturing facility in Hyderabad

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CuraTeQ Biologics successfully completes Phase 1 trial for Omalizumab biosimilar
Press Release

15 March 24

CuraTeQ Biologics successfully completes Phase 1 trial for Omalizumab biosimilar

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Auro Peptides completes US FDA inspection with zero observations
Press Release

17 February 24

Auro Peptides completes US FDA inspection with zero observations

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CuraTeQ Biologics’ Trastuzumab Biosimilar receives recommendation for marketing authorization in India
Press Release

17 January 24

CuraTeQ Biologics’ Trastuzumab Biosimilar receives recommendation for marketing authorization in India

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CuraTeQ Biologics eyes ‘WuXi’ moment to kickstart Indian bio-CDMO sector
Press Release

20 November 23

CuraTeQ Biologics eyes ‘WuXi’ moment to kickstart Indian bio-CDMO sector

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CuraTeQ Biologics to market Ustekinumab biosimilar to treat Crohn’s disease, arthritis
Press Release

10 July 23

CuraTeQ Biologics to market Ustekinumab biosimilar to treat Crohn’s disease, arthritis

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CuraTeQ Biologics announces positive Phase-3 results for Trastuzumab biosimilar
Press Release

05 July 23

CuraTeQ Biologics announces positive Phase-3 results for Trastuzumab biosimilar

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