Attending the right conference can be a turning point for those working in the medical device industry. You may strike up a new business partnership, establish new network connections and, of course, acquire new knowledge about medical devices, quality, regulatory…
Managing informed consent and other types of consent is a vital component of clinical studies, ensuring compliance with regulations, protecting participant rights, and facilitating clear communication. However, traditional consent processes are time-consuming, cumbersome, and difficult to scale. With the 2024.2…
Compliance with industry regulations and standards is a fundamental part of Medtech. Without proper medical device compliance, companies risk harming patients, litigation, and reputational damage. Fortunately, compliance with medical device regulations and standards is not an impossible task. A company-wide…
One impactful way for companies to reduce their carbon footprint is by converting their office/ factory energy consumption from conventional to renewable sources, to adopt sustainable practices. Transitioning to renewable energy can be a powerful step, offering both environmental and…
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