What is a key element of good publication practice enforced during a CIA?

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A key element of good publication practice during a Clinical Investigator Agreement (CIA) is compliance with ethical publication standards. This adherence ensures that all published materials are accurate, transparent, and uphold the integrity of the scientific process. Ethical publication standards serve to protect the interests of patients, sponsors, and the scientific community, promoting accountability and trust in published research.

Ensuring compliance with these standards includes proper attribution of authorship, unbiased reporting of results, and avoidance of plagiarism or manipulation of data, which are all essential for maintaining credibility in scientific literature. Ethical practices in publication are vital for the dissemination of reliable information, allowing stakeholders—including researchers, clinicians, and patients—to make informed decisions based on trustworthy data.

The other options do not represent a commitment to good publication practices: increasing marketing expenses does not relate to the ethical dimensions of publication, reduction in clinical trial reporting contradicts the need for transparency, and promoting competitive practices may lead to selective reporting and bias instead of fostering integrity in scientific communications.

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