Our laboratory has tailor made equipment for Novelia and a dedicated team with extensive expertise on the device. Nemera can conduct customized studies in standard and extreme conditions, as well as generate data to assess compatibility of the combination product, ready to use for registration. Data can also be generated to demonstrate the combination product’s safety and compliance with the highest microbiological safety requirements.
We develop clear and concise instructions for use, in both paper and digital formats, tailored to the specifics of patient populations and drug products. Additionally, we develop user-friendly secondary packaging that is visually appealing while aligning with our customers’ brand values. This comprehensive approach ensures a seamless and supportive experience with Novelia.
We develop customized human factors strategies and risk management plans. We then leverage our expertise in formativeand summative usability testing to ensure customer applicationsmeet user needs and comply with global regulatory standards. Furthermore, when required, we provide human factors engineering documentation for regulatory submissions, enhancing the safety, usability, and overall satisfaction of your product when utilizing Novelia.
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