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Small Molecule CDMO Services Small Molecule CDMO Services

Small Molecule CDMO Services

As a trusted partner in small molecule CDMO space, Aurigene combines expertise, advanced facilities, and a commitment to quality, driving your project from discovery to market.

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.

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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.

Why Aurigene Pharmaceutical Services?

20+

years’ experience

900+

scientists

125+

global clients

600+

projects

19

NCEs
commercialized

16

USFDA inspected
cGMP facilities

6

Biologics
commercialized

3

manufacturing countries
UK, 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
*CTO - Chemical Technical Operations

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
*FTO - Formulation Technical Operations

Virtual Tour

 

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.

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