Aurigene brings over 25 years of expertise in small-molecule CDMO solutions, providing a streamlined, end-to-end approach to meet your development and manufacturing needs.
Our fully integrated services guide you from early-stage development through to regulatory approval, ensuring your project aligns with global standards and achieves successful market entry. Equipped with advanced cGMP facilities and a 4,100 m³ capacity, we manage projects of all scales, delivering high-quality outcomes on time and within scope.
Our team of 700+ skilled scientists has completed over 400 projects, combining technical insight with practical experience to drive your vision forward. Partnering with Aurigene means choosing a dedicated team committed to excellence, precision, and your project’s success every step of the way.
Our Small Molecule Development and Manufacturing Services:
Aurigene Pharmaceutical Services offers specialized small molecule development with capabilities in process optimization, solid form screening, and high-containment handling. Our advanced facilities support complex chemistries, including cryogenic and high-pressure reactions, as well as continuous manufacturing for efficient scaling. With dedicated support for peptides, steroids, and mPEG derivatives, our process development labs and containment facilities ensure precision and safety at every stage. Aurigene ensures a seamless pathway from early development through to large-scale manufacturing, offering smooth tech transfer, in-depth analytical development, and robust IP and regulatory support for reliable market readiness.
Development Services
Manufacturing Services
Specialized Chemistry
Why Aurigene Pharmaceutical Services?
20+
years’ experience
900+
scientists
125+
global clients
600+
projects
19
NCEscommercialized
16
USFDA inspectedcGMP facilities
6
Biologicscommercialized
3
manufacturing countriesUK, Mexico, India
Our Global Manufacturing Footprint
Drug Substance cGMP Facilities
- CTO-Mexico: Large-scale small molecule APIs, steroids and mPEG Alcohol
- CTO-Mirfield: Small molecule, prostaglandin and mPEG derivatives
- CTO-1, India: High potent and small molecule APIs
- CTO-2, India: Small molecule APIs and Nutraceuticals
- CTO-3, India: Low and medium scale small molecule APIs
- CTO-5, India: Large-scale small molecule APIs
- CTO-6, India: Small molecule, peptide, spray drying and high potent
- CTO-SEZ, India: Small molecule, continuous manufacturing, spray drying and high potent
Drug Product cGMP Facilities
- FTO-2: Regular OSDs (oral solid dosage forms)
- FTO-3: Regular OSDs
- FTO-7: Cyto parenterals and cyto and harmonal OSDs
- FTO-9: Non- cyto parenterals ophthalmics and BFS
- FTO-11: Parenterals cyto and non-cyto
- FTO-PU1: Regular OSDs
- FTO-PU2: Topicals, soft gelatin, and potent OSDs
Virtual Tour
Hyderabad R and D Center
Bangalore R and D Center
Connect with our scientific experts for your drug discovery, development, and manufacturing needs
We understand that clear communication is essential to successful collaborations, and that's why we have a dedicated team that is always ready to help you. Whether you have questions about our services, want to discuss a potential partnership, or simply want to learn more about our company, we're here to help.
Our team of experts is dedicated to providing personalised solutions tailored to your unique needs. So, please don't hesitate to reach out to us. We look forward to hearing from you and helping you achieve your business goals.
Resources
FEBRUARY 25, 2025
Transforming Drug Discovery with Aurigene.AI
In the early 2000s, developing Sovaldi, a hepatitis C treatment, took over a decade and nearly $2 billion. Similarly, Zolgensma, a gene therapy for spinal muscular atrophy, required 15 years due to its complexity. However, the advent of artificial intelligence (AI) has revolutionized drug discovery. For example, in 2022, Pfizer's PAXLOVID, an oral COVID...
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Advancement in personalized medicine and how the CRDMO industry is part of the solution
Personalized medicine is transforming the healthcare landscape by customizing treatment plans to individual patients’ unique genetic, clinical and environmental characteristics. These are effective and less invasive treatments for a wide range of conditions. Contract Research, Development and Manufacturing Organizations (CRDMOs) play an important role...
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Cell Line Development
We enable development of stable and high yielding recombinant Mammalian and Microbial lines. ...
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Familiarization, process optimization, and cGMP manufacturing and supply of 30.0 kg of a Bioactive Nucleotide (NAD Booster)
Background: A US-based biopharmaceutical company approached Aurigene Pharmaceutical Services for the familiarization, process development, and cGMP manufacturing and supply of 30.0 kg Nucleotide product (NAD booster) for phase-appropriate studies. The synthesis of the desired product involves three linear stages, which starts with reaction of a pentose...
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Identification of Degradants of Thermal and Oxidation Stress Studies of Empagliflozin and Linagliptin Tablets by HPLC-PDA and LC-MS Instrumental Techniques
2022
Objective of the manuscript is to identify the degradants observed in the thermal and oxidation degradation sample of Empagliflozin and Linagliptin tablets by using LC-MS and HPLC-PDA instrumental techniques. Thermal and oxidation degradation samples were injected in HPLC-PDA and LC-MS instruments. Mass of the degradants were detected by LC-MS technique, ...
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Discovery of MAP855, an Efficacious and Selective MEK1/2 Inhibitor with an ATP-Competitive Mode of Action.
2005
Mutations in MEK1/2 have been described as a resistance mechanism to BRAF/MEK inhibitor treatment. We report the discovery of a novel ATP-competitive MEK1/2 inhibitor with efficacy in wildtype (WT) and mutant MEK12 models. Starting from a HTS hit, we obtained selective, cellularly active ...
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Wang-OSO3H catalyzed green synthesis of bioactive isoindolo[2,1- a ]quinazoline-5,11–dione derivatives: An unexpected observation
2005
The sulphonic acid-functionalized Wang resin (Wang-OSO3H) was explored as a polymeric and recov- erable acidic catalyst for the synthesis of isoindolo[2,1- a ]quinazoline-5,11–dione derivatives under green conditions. Thus the Wang-OSO3H ...
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Polycyclic Aromatic Compounds: A Simple and Efficient [(n-Bu3Sn)2MO4]n Catalyzed Synthesis of Quinazolinones and Dihydroquinazolinones
2005
A novel unprecedented approach for the synthesis of various quinazolinones and dihydroquinazolinones has been using [(n-Bu3Sn)2MO4]n as a catalyst. The reaction has been screened ...
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