Steriles

We recognise that developing sterile dosage forms presents unique challenges. From increasingly stringent regulatory requirements to the complexities of formulation, manufacturing and sterile fill finish, bringing a sterile product to market requires expertise, precision and a deep understanding of the process.

At Meribel, we’re your trusted partner in navigating these complexities. Our experienced team provides comprehensive support throughout your product’s lifecycle, from the initial development stages to the final regulatory submission.

We specialise in the development and manufacturing of a broad range of sterile forms, including:

• Multidose formulations (preservative-free and -containing, including nasal sprays and eyedrops)
• Liquid solutions
• Suspensions
• Sterile injectables
• Sterile lyophilised products
• Preservative-containing formulations.

We’re committed to providing flexible and adaptable solutions, working closely with you to optimise your development and manufacturing processes to ensure the highest quality standards for your sterile products.

Our dedicated quality and regulatory teams are here to support you at every stage, from development to commercialisation, offering:

• Comprehensive support in navigating the regulatory landscape of sterile products
• Accurate and efficient preparation of all necessary documentation for regulatory submissions
• Proactive support, identifying potential challenges and offering solutions to ensure compliance and streamline timelines.

Our goal is to not only meet your expectations but to exceed them, delivering exceptional quality and regulatory support for your sterile product.