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Neuraxpharm owns and operates two global manufacturing companies based in Spain – Lesvi and Inke. The two companies collaborate with industry partners across more than 50 countries and draw on Neuraxpharm’s expertise in CNS and respiratory diseases.
Lesvi focuses on the development and manufacturing of finished dosage forms (FDFs) in mainly solid oral dosage forms and offers a full manufacturing service for customised FDF pharmaceuticals, based upon our own developments.
Inke focuses on the development and manufacturing of the highest quality active pharmaceutical ingredients (APIs) with complex synthesis processes and has more than 20 years’ experience in micronisation.
Neuraxpharm’s Lesvi plant specialises in the development and manufacturing of oral solid and sterile forms, mainly in the CNS area. Its portfolio also includes antiemetic, anti-infective, cardiovascular, pain and respiratory products.
Lesvi’s highly flexible approach and extensive experience have enabled it to cement its place as a reliable partner for large national and international third-party laboratories.
It offers contract manufacturing services for fast dissolving (orodispersible) tablets, using lyophilization techniques.
The company has around 200 employees with teams focused on quality control, materials technology, contract manufacturing, quality assurance, engineering, logistics, safety and environment, and production.
Lesvi has a long history of successfully developing dossiers of generic and specialised pharmaceuticals that meet the latest high regulatory standards. Those dossiers can be licensed from Lesvi, including FDFs with customised artwork designed for specific market needs.
Lesvi has international authorisation for tablets, capsules, powders and injectables.
Successful internal/external audits
High regulatory performance
More than 125 granted patents in the most important countries worldwide
More than 220 dossiers (FDF) submitted to regulatory agencies of different territories
The company focuses on the development and manufacture of high‐added-value active substances for the pharmaceutical industry for use in respiratory and CNS therapies.
Inke has been developing, patenting and implementing its own synthetic routes and polymorphs for the manufacture of active pharmaceutical ingredients since 1980.
Inke is a leading manufacturer in respiratory APIs thanks to its proven success in meeting the high technical and regulatory requirements for each customer, and the company is a key supplier to major generic and branded companies worldwide.
Inke has expertise in high-added-value active substances with complex synthesis processes and its multipurpose plant is designed to meet the stringent standards required for parenteral-grade respiratory and CNS products.
It has more than 20 years’ experience in in-house micronisation technology, purpose-built to ensure quality results from customised products.
Inke has been successfully inspected by every major global authority for its wide range of products, including a US-FDA inspection in April 2019. It holds EU-GMP, ISO 9001, ISO 14001 certifications and Certificates of Suitability (CEPs).
Strong worldwide reputation and brand image
Expertise in customising products (PSDs) to meet each client’s technical and regulatory needs
Working with leading companies across Europe, the US, Japan, Korea and China.
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