In NOMAD, titanium and zirconia were selected as candidate materials for dental implants, and various surface modification strategies were applied to enhance their properties, with WP1 focusing on the development of biological coatings and WP2 on the implementation of smart release concepts for antimicrobial agents. A workflow for sample sterilization has been established, and samples are being evaluated for biomechanical stability following relevant ISO standards in WP3. This includes testing durability against sterilization and forces exerted during implantation and use, ensuring long-term stability of the dental implants. In WP4, experimental protocols for cytotoxicity testing have been established, and samples are undergoing initial screening to guide the biomaterial development. Advanced in vitro models have been optimized, and the first samples have been analyzed using co-culture models. Further sample transfer and evaluation are ongoing. Preparations are being made to scale up production and generate preclinical efficacy data withing WP5 in the next phase of the project. Finally, in WP6, a detailed cost-benefit analysis for the new dental implant biomaterials is underway, including regulatory analysis and technology transfer options.