years of
42 +
Years of chemistry expertise
USFDA Inspection
18 +
USFDA inspection with zero critical observations
Innovator NCE programs
150 +
NCE programs
cGMP Manufacturing facilities
3
cGMP manufacturing facilities in Hyderabad

CDMO Capabilities

We provide drug substance development and manufacturing services across the entire lifecycle — helping you seamlessly transition from early development and clinical trials to commercial GMP supply.

Small Molecules

Robust process development and manufacturing for complex, high value APIs across clinical and commercial stages — including GMP manufacturing for regulated markets.

Peptides (SPPS / LPPS / Hybrid)

Integrated peptide development and manufacturing solutions supporting early phase programs, clinical trials, and commercial supply using flexible technology platforms.

Custom Synthesis

Tailored development of non infringing routes for complex molecules, with a focus on impurity control, reproducibility, and scalability for both clinical and commercial requirements.

Process Development & Scale-Up

From route scouting and feasibility to scale-up for clinical trials manufacturing, ensuring a smooth transition into validated GMP manufacturing.

GMP Manufacturing (Clinical to Commercial)

Global standard GMP manufacturing (USFDA & EU GMP compliant) supporting Phase I–III clinical supply as well as long term commercial production.

What Sets Neuland Apart

A trusted partner for innovators seeking CDMO pharma manufacturing, clinical development support, and scalable commercial supply

 

42+ Years of Complex Chemistry Experience

Specialists in complex small molecules, Peptide APIs and niche therapeutic areas

Integrated Capabilities

Seamless support from early development and clinical trials to commercial GMP manufacturing

Regulatory Excellence

Strong track record of zero observation audits and global regulatory compliance

Innovation Driven

Continuous investment in technology, people and sustainable solutions

Evaluate Your Molecule With Us

Discuss your clinical trials manufacturing, scale up, or GMP manufacturing requirements with our scientific experts.

Whether you're looking to outsource drug manufacturing, optimize your process, or scale to commercial supply — we provide the expertise and infrastructure to support your program.

Confidential technical discussion • No obligation • NDA available on request

CDMO Insights: From Development to Commercial Success

CDMO API Manufacturing for Complex Molecules

CDMO API Manufacturing for Complex Molecules

Read the blog
How CDMO Partnerships Improve R&D ROI for Biopharma Companies

How CDMO Partnerships Improve R&D ROI for Biopharma Companies

Read the blog
From IND to Commercial: How Neuland Ensures Phase-Appropriate Development

From IND to Commercial: How Neuland Ensures Phase-Appropriate Development

Read the blog