Overview
With each significant achievement, we have made an enduring impression on our path towards becoming a widely respected organisation. Our goal is to be a valuable collaborator for the pharmaceutical industry as they strive to improve people's lives while prioritising our responsibility to impact the communities we serve positively.
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2001
Land purchase and Construction of Block I & II.
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2005
Started Manufacturing APIs.
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2005
Commissioning of Block I & II.
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2010
Commissioning of Block III.
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2014
1st USFDA Inspection.
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2015
Commissioning of Block IV, USMDF of 10-DAB III and CEP of Digoxin.
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2016
2nd & 3rd USFDA Inspection and 1st EDQM Inspection.
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2018
4th USFDA Inspection and NMPA approval for Digoxin.
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2019
Commissioning of Block V.
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2021
2nd EDQM Inspection (Remote).
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2025
5th USFDA Inspection (0 Observations).
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2025
Successful CFDI (China) Inspection.
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2026
Filled dossier for Cabergoline CEP at EDQM.
