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Biomedical engineers should base their designs and processes on the best available evidence, ensuring that their work is grounded in rigorous science and clinical research.

Products should be designed to be usable by the widest range of people, considering factors such as accessibility, usability, and inclusivity within the design process.

Biomedical engineers developing data systems must ensure the protection of personal health information, requiring secure data handling protocols and adherence to privacy laws.

Use of animals in testing must be necessary, and efforts should be made to minimize suffering and use alternatives when possible, reflecting on the ethical use of animals.

Engineers must respect and protect intellectual property rights while encouraging innovation, which involves navigating patent laws and licensing agreements.

Biomedical engineers must foster collaborative relationships with healthcare professionals to ensure that designs meet clinical needs and enhance the efficacy of healthcare delivery.

Biomedical innovations should be accessible to all societal groups, avoiding discrimination. Engineers should consider cost, distribution, and barriers to access.

Engineers should commit to ongoing learning to keep up with technological advances and evolving ethical standards, which ensures continued professional competency and ethical practice.

Biomedical engineers must maintain high standards of competence and undertake tasks only within their expertise, which has implications for ongoing education and certification.

Biomedical innovations should align with public health goals, aiming to improve overall health outcomes, address health disparities, and considering the impact on healthcare systems.

Clinical trials must avoid causing harm to participants, including long-term and short-term effects. Biomedical engineers must prioritize safety in the design and testing phases.

Biomedical solutions must be culturally sensitive to be effective and accepted in different regions, requiring research and consideration of local customs, languages, and needs.

Participants in biomedical research must be fully informed of the risks, benefits, and purposes of the study to give voluntary consent. Implications include clear communication and ethical review board oversight.

Engineers must participate in peer review to ensure research quality and credibility, remaining impartial and confidential during the review process.

Biomedical innovations must be economically feasible, with engineers considering both the cost of development and the financial impact on healthcare systems and patients.

Biomedical engineers should respect patient autonomy in the development of devices and systems, while also considering when professional guidance might override patient preferences for health outcomes.

Biomedical engineers must conduct thorough risk-benefit analyses for new products to determine if the benefits outweigh potential risks, adhering to regulatory standards and best practices.

Designers must ensure biomedical devices contribute to the welfare of patients by improving health outcomes, minimizing pain, and reducing recovery time. Implications include rigorous testing for effectiveness and safety.

Biomedical engineers must report data and research findings honestly, without fabrication, falsification, or plagiarism, maintaining the integrity of scientific literature.

When developing algorithms for biomedical applications, engineers must strive for transparency to allow understanding of decision-making processes, which affects trust and adoption rates.

Engineers are accountable for their work's impact on patients and society, necessitating error reporting, transparent practices, and ethical decision-making.

Biomedical research with potential for both beneficial and harmful applications must be managed to minimize risk of misuse, involving ethical decision-making and possibly government oversight.

Biomedical engineers must consider how their work affects resource allocation in healthcare settings, striving for solutions that optimize resource use without compromising care quality.

Biomedical professionals must disclose any financial or personal interest that might influence their research outcomes, clinical judgements or professional decisions.