Speakers at MediaNama's event on draft DPDP Rules discussed consent notices, data summaries, and how companies should approach compliance.

Intensive Training Course on Pre- and Post-Market StudiesDublin, Feb. 05, 2025 (GLOBE NEWSWIRE) -- The "Medical Device Studies: Clinical Evidence Training Course (ONLINE EVENT: April 7-8, 2025)" has ...

These are tools used by the IRB and are not required to be used/submitted by investigators. Research teams may find them helpful when writing protocols to more clearly understand what the IRB must ...

(CNN) – The U.S. Food and Drug Administration approved the first new type of pain medication in more than two decades, and it’s not an opioid. The drug is suzetrigine under the brand name ...

These medications contain various forms of amphetamine or methylphenidate and have a calming effect. They work by increasing levels of dopamine and norepinephrine in the brain. Dopamine and ...

Administration routes are based on the medication used, how quickly it needs to be absorbed, and the part of the body where the medication needs to have an effect. Your healthcare provider or ...

Eligible studies included surveys, focus groups, or interviews. Based on a review of consent form templates, we identified 18 elements that commonly appear in consent forms, and used these to guide ...

Children at a Dublin creche were given medication without ... available five of the [15] forms were not completed appropriately and did not contain signed parental consent,” said the report.

Iraq has passed a law that would legalise the marriage of children as young as nine. Three divisive laws have now been passed which give Islamic courts increased authority over family matters ...

Before the advent of medications, individuals with these more extreme symptoms often found themselves stuck—unable to engage meaningfully in therapy or, in many cases, requiring long-term ...