As a first-class European CDMO partner in the field of biotech pharmaceutical contract manufacturing of sterile drugs, specialised in fill and finish services of multiple formats of vials for injection and plastic bottles (eye drop type), we use our expertise in Pharmaceutical R&D, Aseptic Filling, Lyophilization of Biologics (including peptides and proteins, antibodies / mAB, RNA, adenovirus, etc.) and extensive knowledge of international requirements to enable your product to meet the most demanding quality standards and thus fulfil customer needs. 

Our facilities, equipped with the latest technologies, are strategically located in a vibrant biopharmaceutical hub in the North of Spain, near prominent research institutions and other relevant partners which help to enhance our capabilities and resources. 

We have experience and expertise in working with major regulatory authorities. Liof Pharma’s own Quality Assurance (QA) system complies with international GMP standards. We undergo regular inspections as part of our commitment to quality and compliance, including successful Pre-Approval Inspections by the FDA. We are a flexible, experienced and customer focused team. We have implemented our own systems to continuously enhance processes and procedures.

Liof Pharma development services offers clinical manufacturing expertise from early-stage development to market launch. Our goal is to serve as your one-stop-shop biotech CDMO from clinical development to commercial manufacturing, covering all aspects from sterile processing to distribution. An experienced Project Manager will oversee every aspect of your project to ensure its success.

Liof Pharma

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