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Bulk Drugs and API Intermediates Manufacturers

Suviro Life Sciences

Founded in 2018, Suviro Life Sciences has established itself as a trusted partner in the manufacturing and procurement of bulk drug intermediates. With a strong focus on compliance, operational excellence, and supplier transparency, we serve pharmaceutical companies, biotech firms, NGOs, and academic institutions worldwide.

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About Us

Suviro Life Sciences was established in the year 2018, as a medium scale industry with limited products. We dedicate ourselves to manufacturing of Pharma Intermediates and APIs meeting the quality standards of National and International customers and committed to work under safe and healthy environment.

Suviro Life Sciences has great respect for knowledge and encourages the talented work force in its organization. Talented employees are in good positions and contributing in a remarkable way to achieve the goals of the organization. All those joining our Suviro family are taught on morals and ethics and then trained to execute their jobs with responsibility.

Our achievements in the last few years have helped the organisation to expand into the global market. Our growth and success is credited to the cooperation and team work of all employees, who have always been our tremendous strength, our suppliers and our valuable customers. Suviro Life Sciences strives and continues to work in the path of moving towards organisational and business excellence and at the same time believes to be an example as a contributor and work towards national aspirations. We believe that we have a lot to achieve and all at Suviro family are dedicated to move forward in this journey.

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Active Pharmaceutical Ingredients

The main ingredient in a medicine that causes the desired effect of the medicine. Some medicines contain more than one active pharmaceutical ingredient that act in different ways in the body. Also called API, drug substance, and pharmacologic substance.

Intermediates

Pharmaceutical intermediates are chemical compounds that are synthesized and used during the production of active pharmaceutical ingredients (APIs). These are intermediate compounds formed at various stages in the synthesis of APIs.

What we do

Products manufactured

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Meta Chloro Anisole

CAS No: 2845-89-8

N,N Carbonyl Di Imidazole (CDI)

CAS No: 530-62-1

Racemic Sertraline

CAS No:79617‑89‑3

4‑Amino Benzo Nitrile

CAS No: 873‑74‑5

4‑(Chloromethyl)‑5‑Methyl‑2‑Oxo‑1,3‑Dioxole

CAS No: 80841‑78‑7

Dibenzoyl‑L‑tartaric acid monohydrate

CAS No: 62708‑56‑9

Our Mission

To provide affordable and quality medication for everyone and to manufacture in a way to balance social, economic, and environmental sustainability.

Our Vision

To build a vertically integrated organization led by innovation to produce the highest quality products.

Sustainability

Employee safety, community engagement, and CSR initiatives.

“We invest in our people and communities, fostering a culture of responsibility and care.”

Office

Flat No:207, Sri Sai Nikethan Apt, AS Raju Nagar, Kukatpally, Hyderabad-500072

Direction

Our Plant-1

Sy no:33, Rayarao Pet Vil, Bibi Nagar mandal, Yadadri Dist, Telangana-508126

Direction

Our Plant-2

PLOT NO: 249 & 250, Badiyal Industrial Area, Kadechur, Saidapur Vil, Yadgir District, Karnataka-585221

Direction
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About Founders

We Are Leading As One of The Intermediates Manufacturer In India

G. Siva Rami Reddy

Director

G.DIneshwara Reddy

Partner

About Us

Managing Director

Guda Siva Rami Reddy, the founder and Managing Director of Suviro Life Sciences, is a seasoned professional with over 27 years of extensive experience in the bulk drug and intermediates industry.
He possesses a deep understanding of the entire product lifecycle, from research and development (R&D) and production to quality control (QC). His hands-on knowledge in these critical areas ensures operational excellence and adherence to the highest standards. In addition to his technical expertise, Mr. Reddy is recognized for his exceptional marketing skills, a crucial asset that has allowed him to navigate the competitive bulk drug market effectively.

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Director

CDr. Guda Dinneswara Reddy is a distinguished scientist and the Director of Suviro Life Sciences  in Hyderabad, India, with vast expertise in synthetic organic and heterocyclic chemistry. His work spans multiple high-tech fields, including drug development, artificial photosynthesis, and the creation of atomic layer deposition (ALD) precursors for the semiconductor industry. Throughout his career, he has held significant research roles in both industry and academia, demonstrating a profound ability to lead innovative projects from concept to application.
His remarkable career is marked by key achievements, including the development of groundbreaking catalysts for sustainable energy applications and novel synthetic methodologies for a variety of heterocyclic compounds. Dr. Reddy holds several patents for his work on ALD precursors for semiconductors and anti-allergy compounds. He is also a widely published author in prestigious scientific journals and has been recognized with multiple honors and awards, such as the IAAM Scientist Medal and the Yonsei Standing Proud Young Researcher Award, underscoring his influential contributions to science and technology.

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OUR FACILITIES

R&D Facilities

Suviro Life Sciences has set up a Research and Development Centre. It has helped us to make a successful entry into an enhanced product portfolio. The R&D Centre facility focuses on generic API and intermediates development. Our AR&D facility is located in Hyderabad.

QC and QA Facilities

As an organisation engaged in a business affecting human lives and upholding moral & ethical values, Suviro Life Sciences strongly believes in manufacturing of high quality products. Suviro aims to maintain and enhance the quality of the products being manufactured across the organisation through continuous process development as per regulatory and customer requirements.

Manufacturing Facilities

Suviro Life Sciences manufacturing facilities including Production blocks, Clean rooms, Warehouse and all utilities are established according to the GMP and FDA requirements and guidelines. We have all the required manufacturing drug licenses and certifications from the relevant authorities.

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