Boonyarat Kanjanapongporn

I agree that keeping consistent format throughout the CRF, would reduce the time consumption when filling the form.

Great point on the impact toward analysis and healthcare, which are resulted from effective data merging.

Thank you for sharing, interesting data management process.

I don’t have experience with clinical research involving data management processes. From the lectures, there are many problems which could affect data quality and regulation compliance from the process of data acquisition to the process of data entry. That is, the regulation or problem including entry errors, system authentication, data a…[Read more]

Thank you for sharing, your infographic look amazing. Interesting point on the inform consent in clinical research and PDPA. I agree with your conclusion and also think that PDPA would wider the application of inform consent in other healthcare related data apart from clinical trial.

Increase in productivity of work processes is the benefit after the standards are implemented. By applying the standards, data will have clear format with unique code of variables. These would save the time on data transferring, because researchers don’t have to reassess a new clinical record format each trial, and data might be automatically t…[Read more]

Comment above did mentioned many good points to improve this CRF. I would suggest amending the open ended question at Physical examination on Abnormal specifying. The blank spaces provided might not be enough for people who have many conditions and the hand writing might be hard to read if the condition is complicated.
Therefore, I suggest the…[Read more]

Thanks for sharing, the QC and QA process wasn’t done in my project which was small as well. I agree to not neglect this part for better research quality.

Thank you for sharing, your research sound interesting. I could imagine how long will it take to get precise answer related to user perception.

Great topic abbreviation! Your infographic has cover many issues and it’s look beautiful.😊

From the discussion previous, I didn’t really have a plan on data management in my medicinal formulation research. Even though it didn’t involve personal data or interviews, a proper plan would have been better. If I could turn back the time, there would be a few steps which I could add to my data management to enhance work quality.

Firstly, bet…[Read more]

I don’t have experience of clinical or public health data collection. However, during my bachelor degree study, I did have to collect data for medical formulation ratio in drug formulation experiments which didn’t involve personal data, yet some processes related to the study of data management.

1. The medical formulation involved repeated exp…[Read more]

Great infographic and abbreviation on AMIA 2018, thank you.

Thank you for sharing the conclusive ideas toward the ethical AI adoption. All of your suggested points are crucial and would lead to the sustainable development.

I agree with yours conclusion on ChatGPT application.

I tried to upload many times and it wasn’t work🥹. Thank you for suggestion, will try again next week.

Great explanation on p value and conclusion. It’s always the need to include other factor which might affect the outcome.