CDMO, aseptic filling and finishing, lyophilisation, sterile medicines, FILL&FINISH, biological medicines, sterile vials.
As a leading European biotech CDMO in the field of contract manufacturing of sterile medicines, specialising in filling and finishing services for multiple formats of injection vials and plastic (eye drop) bottles, we use our expertise in pharmaceutical R&D, aseptic filling, freeze drying of biologics (including peptides and proteins, antibodies/mAB, RNA, adenovirus, etc.) and extensive knowledge of international requirements to enable your product to meet the highest quality standards, thus satisfying your customer’s needs. ) and extensive knowledge of international requirements to enable your product to meet the highest quality standards, thus satisfying customer needs.
Our facilities, equipped with the latest technologies, are strategically located in a vibrant biopharmaceutical hub in Northern Spain, close to leading research institutions and other relevant partners, which helps to enhance our capabilities and resources.
We have experience working with the main regulatory authorities. LIOF PHARMA has a proprietary Quality Assurance (QA) system that complies with international GMP standards. We undergo regular inspections as part of our commitment to quality and regulatory compliance, including a successful FDA pre-approval inspection. We are a flexible, experienced and customer-focused team. We have implemented our own systems to continuously improve processes and procedures.
LIOF PHARMA’s pharmaceutical development services provide clinical manufacturing expertise from early stage development to market launch. We aim to serve as your one-stop biotech CDMO, spanning from clinical development to commercial manufacturing and covering all aspects from sterile processing to distribution. An experienced project manager will oversee every aspect of your project to ensure its success.
DESCRIPTION:
As a leading European biotech CDMO in the field of contract manufacturing of sterile medicines, specialising in filling and finishing services for multiple formats of injection vials and plastic (eye drop) bottles, we use our expertise in pharmaceutical R&D, aseptic filling, freeze drying of biologics (including peptides and proteins, antibodies/mAB, RNA, adenovirus, etc.) and extensive knowledge of international requirements to enable your product to meet the highest quality standards, thus satisfying your customer’s needs. ) and extensive knowledge of international requirements to enable your product to meet the highest quality standards, thus satisfying customer needs.
Our facilities, equipped with the latest technologies, are strategically located in a vibrant biopharmaceutical hub in Northern Spain, close to leading research institutions and other relevant partners, which helps to enhance our capabilities and resources.
We have experience working with the main regulatory authorities. LIOF PHARMA has a proprietary Quality Assurance (QA) system that complies with international GMP standards. We undergo regular inspections as part of our commitment to quality and regulatory compliance, including a successful FDA pre-approval inspection. We are a flexible, experienced and customer-focused team. We have implemented our own systems to continuously improve processes and procedures.
LIOF PHARMA’s pharmaceutical development services provide clinical manufacturing expertise from early stage development to market launch. We aim to serve as your one-stop biotech CDMO, spanning from clinical development to commercial manufacturing and covering all aspects from sterile processing to distribution. An experienced project manager will oversee every aspect of your project to ensure its success.
Keywords:
CDMO, aseptic filling and finishing, lyophilisation, sterile medicines, FILL&FINISH, biological medicines, sterile vials.
