Successfully completed US FDA Remote Regulatory Assessment at our Analytical Testing Facility (CLAS)
Successfully commercialized Remdesivir & Favipiravir which were authorized in emergency treatment of Covid-19.
Dedicated Ibupforen manufacturing block inaugurated.
Successfully completed EU GMP inspection by EDQM at our Bachupally facility.
Successfully completed 3rd US FDA inspection at our Vijayanagaram facility.
Successfully completed 1st US FDA inspection at our Analytical Testing Facility (CLAS)
Central Laboratory Analytical Services (CLAS) established to cater analytical services using hyphenated analytical techniques.
Demerged SMS group into 2 Entities – SMS Pharmaceuticals, SMS Lifesciences.
Successfully completed PMDA- Japan inspection at our Bachupally facility.
Successfully completed 5th US FDA inspection at our Bachupally facility.
Successfully completed 2nd US FDA inspection at our Vijayanagaram facility.
Won the prestigious “Indian Pharma Bulk drug company of the year” award and “Best bulk drug export company of the year” award from Govt. of India.
Renewal of EU-GMP certification by Hamburg Health Authority (BGV) is successful at our Bachupally facility.
Successfully completed 4th US FDA inspection at our Bachupally facility.
Commercial production started in our world class API facility, Vijayanagaram.
Successfully completed 1st US FDA inspection at our Vijayanagaram facility.
Successfully completed 3rd US FDA inspection at our Bachupally facility.
EU-GMP certification by Hamburg Health Authority (BGV) is successful at our Bachupally facility.
Started a green field project to build an API facility in more than 100 acres of Land.
DSIR recognized our Gagillapur R&D center.
Successfully completed 2nd US FDA inspection at our Bachupally facility.
Inauguration of state of the art R&D Center at Gagillapur, Hyderabad.
SMS got listed on the NSE, BSE (Indian stock exchange) – Public Listed company.
DSIR recognized our in-house R&D center.
In-house R&D center established at Sanath Nagar, Hyderabad.
Faced our first USFDA audit (successfully); SMS API was Part of a Para IV filing from an MCN company.
Successfully commercialized Sumatriptan Succinate at our Bachupally facility.
Recognized by govt. of India with a Jawaharlal Silver rolling trophy for the best productivity of the year.
Became the Largest manufacturer of Ranitidine API in the world.
SMS Pharma was started with single Unit, single product facility.
Successfully completed US FDA Remote Regulatory Assessment at our Analytical Testing Facility (CLAS)
Successfully commercialized Remdesivir & Favipiravir which were authorized in emergency treatment of Covid-19.
Dedicated Ibupforen manufacturing block inaugurated.
Successfully completed EU GMP inspection by EDQM at our Bachupally facility.
Successfully completed 3rd US FDA inspection at our Vijayanagaram facility.
Successfully completed 1st US FDA inspection at our Analytical Testing Facility (CLAS)
Central Laboratory Analytical Services (CLAS) established to cater analytical services using hyphenated analytical techniques.
Demerged SMS group into 2 Entities – SMS Pharmaceuticals, SMS Lifesciences.
Successfully completed PMDA- Japan inspection at our Bachupally facility.
Successfully completed 5th US FDA inspection at our Bachupally facility.
Successfully completed 2nd US FDA inspection at our Vijayanagaram facility.
Won the prestigious “Indian Pharma Bulk drug company of the year” award and “Best bulk drug export company of the year” award from Govt. of India
Renewal of EU-GMP certification by Hamburg Health Authority (BGV) is successful at our Bachupally facility.
Successfully completed 4th US FDA inspection at our Bachupally facility.
Commercial production started in our world class API facility, Vijayanagaram.
Successfully completed 1st US FDA inspection at our Vijayanagaram facility.
Successfully completed 3rd US FDA inspection at our Bachupally facility.
EU-GMP certification by Hamburg Health Authority (BGV) is successful at our Bachupally facility.
Started a green field project to build an API facility in more than 100 acres of Land.
DSIR recognized our Gagillapur R&D center.
Successfully completed 2nd US FDA inspection at our Bachupally facility.
Inauguration of state of the art R&D Center at Gagillapur, Hyderabad.
SMS got listed on the NSE, BSE (Indian stock exchange) – Public Listed company.
DSIR recognized our in-house R&D center.
In-house R&D center established at Sanath Nagar, Hyderabad.
Faced our first USFDA audit (successfully); SMS API was Part of a Para IV filing from an MCN company.
Successfully commercialized Sumatriptan Succinate at our Bachupally facility.
Recognized by govt. of India with a Jawaharlal Silver rolling trophy for the best productivity of the year.
Became the Largest manufacturer of Ranitidine API in the world.
SMS Pharma was started with single Unit, single product facility.
| 2021: Successfully commercialized Remdesivir & Favipiravir which were authorized in emergency treatment of Covid-19. |
| 2021: Dedicated Ibupforen manufacturing block inaugurated. |
| 2022: Successfully completed US FDA Remote Regulatory Assessment at our Analytical Testing Facility (CLAS). |
| 2016: Received prestigious “India Pharma Bulk Drug Company of the Year” & “Bulk Drug Export Company of the Year” awards from Govt. of India. |
| 2017: Demerged SMS group into two separate entities - SMS Pharmaceuticals & SMS Life Sciences. |
| 2017: Successfully completed PMDA- Japan inspection at our Bachupally facility. |
| 2017: Successfully completed 5th US FDA inspection at our Bachupally facility. |
| 2019: Central Laboratory Analytical Services (CLAS) established to cater analytical services using hyphenated analytical techniques. |
| 2020: Successfully completed EU GMP inspection by EDQM at our Bachupally facility. |
| 2020: Successfully completed 3rd US FDA inspection at our Vijayanagaram facility. |
| 2020: Successfully completed 1st US FDA inspection at our Analytical Testing Facility (CLAS) |
| 2011: Successfully completed 3rd US FDA inspection at our Bachupally facility. |
| 2011: EU-GMP certification by Hamburg Health Authority (BGV) is successful at our Bachupally facility. |
| 2012: Commercial production started in our world class API facility, Vijayanagaram. |
| 2012: Successfully completed 1st US FDA inspection at our Vijayanagaram facility. |
| 2014: Renewal of EU-GMP certification by Hamburg Health Authority (BGV) is successful at our Bachupally facility. |
| 2014: Successfully completed 4th US FDA inspection at our Bachupally facility. |
| 2015: Successfully completed 2nd US FDA inspection at our Vijayanagaram facility. |
| 2007: We went public and were listed on BSE & NSE. |
| 2008: Successfully completed 2nd US FDA inspection at our Bachupally facility. |
| 2008: Inauguration of state of the art R&D Center at Gagillapur, Hyderabad. |
| 2009: DSIR recognized our Gagillapur R&D center. |
| 2010: Vijayanagaram API facility - A green field project spanning across 100 acres of land is proposed to build. |
| 2001: Successfully commercialized Sumatriptan Succinate at our Bachupally facility. |
| 2003: Received our 1st USFDA approval for the API Sumatriptan Succinate, which continues to be one of our best-known product worldwide. |
| 2004: In-house R&D center established at Sanath Nagar, Hyderabad. |
| 2005: DSIR recognized our in-house R&D center. |
| 1997: Recognized by the Govt. of India with a “Pandit Jawaharlal Nehru Silver Rolling Trophy” award for the best productivity efforts. |
| 2000: Acquired a facility (Unit-II, Bachupally) and upgraded to manufacture niche and high value products to have a diversified portfolio. |
| 1989: Started our journey with Ranitidine, as a single product facility. |
| 1995: Became the largest manufacturer of Ranitidine API in the world. |