Our deep understanding of complex chemical processes and manufacturing has enabled us to build a strong track record in delivering exclusive custom manufacturing solutions.

We manufacture intermediates and APIs for commercial novel molecules, covered under patent protection and can scale up for commercial supplies.

We provide lab, kilo and pilot scale manufacturing support across the lifecycle of your product, supplying drug quantities for preclinical studies through all phases of clinical trials (milligram to kilogram) to product launch and in-market supply (kilogram to 100+ metric ton).

Our skilled scientists and our ability to adapt to each stage of the development process, ensuring smooth transitions as manufacturing requirements increase, have made us a trusted partner for pharmaceutical and biotech customers.

Clinical Manufacturing

Clinical manufacturing

In any clinical trial, it is essential that the drug is produced from reliable regulatory starting materials (RSMs)

We work closely with our customers to understand their clinical development plans and provide a bespoke clinical manufacturing solution. Our stringent processes and highly trained scientists ensure that quality standards are maintained throughout each clinical phase. 

At Neuland, we have the facilities and capabilities to produce APIs for Phase I through to large Phase III clinical trials. Our team has the knowledge and expertise to support you at every step of the clinical manufacturing process.   

Commercial manufacturing

Our experienced and agile team works with you to overcome the challenges of commercial manufacturing. We see ourselves as an extension of our customers’ teams and are invested in their projects and the journey to commercial production.

We are reliable and flexible, ready to assist you on your journey to commercialization and help you overcome whatever obstacles may occur in a changing market.

As a contract manufacturing organization for the past 40 years, our specialty has been small molecule API manufacturing at all phases, from preclinical to commercial. We have a proven track record of supplying APIs built on safe and robust processes, in regulatory compliant facilities.

Our technology transfer process guarantees a seamless scale-up from development through to commercial production.

Commercial Manufacturing
Custom Development

Custom Development

Discover our end-to-end continuum of customised chemistry services at every stage of drug development cycle.
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Phase Appropriate Development

Phase Appropriate Development

How we handle a range of chemistry services from pre-IND through to manufacturing.
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cDMO

CDMO Brochure

Explore the services we offer in small molecule development and manufacturing.
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