SETV Global - CDMO/CMO

We are a company that creates treatments and chemical intermediates that can fasten the drug process and various other pharmaceutical applications and products. We primarily invest in and develop various process methods to reduce the drug delivery time and shorten the whole process. This happens with our advanced intermediates and process plans. "Cause when it matters the most, we are always there".

Introducing our suite of innovative services: At the forefront of pharmaceutical advancements, we specialize in crafting cutting-edge treatments and chemical intermediates designed to expedite the drug development process and advanced intermediates.

We are unique in:

Robust Analytical Capabilities
Equipped with state-of-the-art
analytical tools like 500 MHz NMR and
LC-MS/MS for precise quality control
and assurance.

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Address: SETV.ASRV LLP, Avishkaran, NIPER, Balanagar, Hyderabad, Telangana, 500037., , Hyderabad
India

Local time:

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API, Intermediates, Building Blocks, Impurities, Amino acids and Peptides

Small quantity APIs to commercial scale

GMP and USFDA certification based on quantity, order, assignment.

Drug Substance

small

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Employees:

Established in:

2021

Drug Substance (CDMO/CRO)

Intermediates

Pharmaceutical intermediates are compounds used in the production of APIs. CDMOs play a crucial role in synthesizing, scaling, and ensuring the quality of these intermediate compounds to support efficient drug manufacturing.

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Small Molecule APIs

Small molecule APIs form the backbone of many pharmaceutical drugs due to their low molecular weight and ease of synthesis. They are widely used in treating a range of diseases and are typically produced through chemical synthesis in GMP-compliant facilities.

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Contact SETV Global for Contract Services Expertise

Connect with SETV Global, a leading pharmaceutical company from India. They offer specialized Drug Substance (CDMO/CRO). Contact SETV Global for free and discover if they are the perfect partner for your pharmaceutical needs.

Drug Substance (CDMO/CRO)

Drug Substance CDMOs and CROs provide essential services in the development and manufacturing of active pharmaceutical ingredients (APIs). These organizations specialize in early-stage research, process development, and GMP-compliant manufacturing of drug substances for clinical and commercial use.

Pharmaoffer's Drug Substance CDMO/CRO category includes partners with expertise in small molecules, biologics, peptides, and complex chemistry, all operating under strict regulatory compliance. These providers help companies scale from lab to market efficiently and cost-effectively.

Key Functions of Drug Substance CDMOs/CROs:

API Research and Development: Providing early-stage discovery support, custom synthesis, and process optimization to streamline the development of drug substances.
Process Scale-Up and Tech Transfer: Transitioning from bench-scale to pilot and commercial scale production with validated methods and reproducibility.
GMP Manufacturing: Delivering high-quality API batches in GMP-certified environments, adhering to FDA, EMA, and other international standards.
Analytical Services: Offering comprehensive analytical method development and validation to ensure consistent quality and regulatory compliance.
Flexible and Specialized Capabilities: From small molecule synthesis to biologic and peptide manufacturing, these partners provide specialized services tailored to product-specific needs.

Explore Leading API CDMOs and CROs

Pharmaoffer connects you with trusted CDMOs and CROs for drug substance development. Our platform enables seamless access to specialized service providers equipped to support your API lifecycle from discovery to commercialization.