Our CRDMO services

Interested in developing liposomal medication? Contact us!

InnoMedica offers you international scientific excellence, along with state-of-the-art GMP infrastructure. The company is distinguished by its modern, modular facilities, featuring cleanrooms that meet Good Manufacturing Practice (GMP) requirements. This advanced research and manufacturing environment ensures the highest standards in the development, production, and quality assurance of your pharmaceutical products.

InnoMedica’s specialists provide expert consultation and, when needed, operational support in the following areas:

Preclinical Development

– Design and concept development of liposomal prototypes (Quality by Design, QbD)
– Manufacture of research and development batches
Clinical Development

- GMP production, aseptic filling, labeling, packaging, quality control, quality assurance, and batch release

- Planning and execution of clinical trials in compliance with GCP

- Preparation and submission of Clinical Trial Applications and protocols (CTA, CTP), as well as protocol amendments
Regulatory Support

- Investigator’s Brochure (IB)

- Pharmaceutical Quality Dossier (PQD)

– eCTD

Flexibility is a core principle of our work. With a modern infrastructure, InnoMedica is well-equipped to collaboratively develop innovative solutions and ensure the success of your projects. Our services can be tailored to meet the specific needs and requirements of our collaboration partners.

If you are interested, feel free to get in touch with Dr. Martin Stähle, CFO of InnoMedica.

martin.staehle@innomedica.com / +41 (0) 31 311 04 27