Our services cover all the pharmaceutical industry’s chemistry requirements. As an experienced Indian CDMO, Neuland has the capabilities to custom develop drug products from molecule through to clinical development and commercial-scale supply with minimal tech transfer timelines.
We offer a range of consulting services through every stage of the development process, from assistance with process development, process optimization, analytical testing, technology transfer, polymorph screening, salt screening, DoE studies and QBD for molecules depending on the phase of the product. In addition to this, Neuland provides CMC support and helps biotech companies utilize the regulatory services.
Chemistry and Process Development
It is essential that the drug substance is safe and effective for its intended use. Process optimization and validation play a pivotal role in ensuring its quality.
Read moreAnalytical Development & Validation
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Process Safety & Engineering Assessment
Process safety is critical in drug substance development to ensure manufacturing processes are safe and reliable. At Neuland, we partner with customers to understand their specific needs and develop customized process safety solutions.
Read morePhase Appropriate Development
Neuland provides full-cycle development and manufacturing solutions. Our scientific experts are equipped to tackle obstacles at every stage of the process throughout the entire development journey as part of your extended team.
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