News
Informed consent in clinical trials: not just a form
It is not an exaggeration to say that patients determine the outcome of the clinical trial since they are the subjects of the research – meaning that their reactions to...
How to combat data errors in clinical trials
Anybody can agree that data lie at the heart of any research, including clinical study. Accurate data allows researchers to make insightful decisions. In case of clinical trials, clean and...
How eClinical changes the face of modern clinical trials
It comes as no surprise to see the prefix e that stands for electronic in this age of flourishing technology, and eClinical is no exception. With the help of constant technical advances, eClinical is...
Four parties in a clinical trial
Most of us hear the term clinical trial on drug advertisements since that’s the compulsory progress a medicine must go through before entering the market. Yet, not many people know the people...
Everything you need to know about adaptive clinical trials
For as long as clinical trials have existed, traditional procedures have been the to-go way to conduct a study. That is, the whole process that normally lasts 10+ years and...
Entering Southeast Asia: Opportunities and barriers awaiting CDM
Most people in Southeast Asia (SEA) will shake their heads when asked about clinical trials, let alone clinical data management (CDM). If eClinical in North American and Western markets is...
A look at clinical trials in Asia: South Korea, Taiwan, India and China
Asia is no doubt the current healthcare hub of the world, with a share of 41.8% in global research and development (R&D) spending in 2016. Since we can all anticipate...
5 things to keep in mind when choosing an EDC system/CDMS
It goes without saying that eClinical is trending as more and more clinical studies seek technical alternatives to traditional paper and spreadsheets. However, among a sea of vendors, it’s often...
