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?

LEARN MORE
Biosimilar Production 2

Biosimilar Research and Development

LEARN MORE
Biosimilar Production 3

Biosimilar Manufacturing Capabilities

LEARN MORE
Biosimilar Production 4

Quality Control Laboratories

LEARN MORE

Latest News

CuraTeQ Biologics successfully completes Phase I study for Denosumab biosimilar
Press Release

10 April 25

CuraTeQ Biologics successfully completes Phase I study for Denosumab biosimilar

Read More
CuraTeQ Biologics receives CHMP positive opinion for Pegfilgrastim biosimilar
Press Release

31 January 25

CuraTeQ Biologics receives CHMP positive opinion for Pegfilgrastim biosimilar

Read More
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)

Read More
CuraTeQ Biologics receives CHMP positive opinion for Filgrastim biosimilar
Press Release

13 December 24

CuraTeQ Biologics receives CHMP positive opinion for Filgrastim biosimilar

Read More
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

Read More
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

Read More
Auro Peptides completes US FDA inspection with zero observations
Press Release

17 February 24

Auro Peptides completes US FDA inspection with zero observations

Read More
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

Read More
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

Read More
Overview
CuraTeQ Biologics

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.

You can adjust your preferences below.

Essential Cookies

Essential Cookies should be enabled at all times so that we can save your preferences for cookie settings. If you disable this cookie, we will not be able to save your preferences. This means that every time you visit this website you will need to enable or disable cookies again.

Google Analytics

This website uses Google Analytics to collect anonymous information such as the number of visitors to the site, and the most popular pages. Keeping this cookie enabled helps us to improve our website.