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Our Comprehensive CDMO Services

Phase	Solution	Capability	Infrastructure
Pre-clinical	Pre-clinical manufacturing Regulatory support	Pre-clinical synthesis Regulatory documentation	R & D and kilo lab Analytical lab
Phases 1–3 (Clinical Development)	Chemistry & process development Analytical method development , validation, method transfers to QC Scale-up & tech transfer Validation & stability studies Support for regulatory filing Hazard identification and risk assessment report APIs manufacturing from class 1,00,000 area Operate at multi products facility	Synthesis labs Method development & impurity profiling Salt & polymorph screening RC1e calorimetry, DSC, TSU, RSD Cryogenic reactions Hydrogenation & cyanation High vacuum distillation Filtration & crystallization Different capacities of equipments with multiple MOCs	Analytical labs (HPLC, GC, LC-MS, XRD, HRMS,NMR) Crystal-16, FBRM, microscope images, cylindrical equipment Kilo lab & pilot plant ATFD, falling film evaporators Structured packed columns for high vacuum distillation. Safety systems (HCN detectors, scrubbers) Various close handling filtration and drying equipment
Commercial	Commercial manufacturing	Large-scale API production Powder processing High vacuum distillation Hazardous chemistry handling Regulatory support	1174 KL reactor capacity Drying/milling/sieving systems Dedicated blocks for hazardous chemistry Regulatory documentation systems

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CDMO Pharma Manufacturing 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.

Commercial Manufacturing

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

Why European & UK Companies Choose Neuland?

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

CDMO support from early phase programs, clinical trials to cGMP manufacturing
USFDA & EU GMP compliant manufacturing facilities
Successfully inspected by USFDA, EMA, PMDA, and other global regulators
Proven experience supporting European biotech and pharma companies across development stages
Trusted partner for companies looking to outsource drug manufacturing with full regulatory support
Strong expertise in complex chemistries, challenging syntheses, and impurity control
Scalable development using QbD and DoE principles to reduce risk across lifecycle stages

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