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trials is in accordance with the CUKB protocol and principles, especially for
researchers and sponsors, she said.
"The implementation of good clinical trials will produce valid data and can be
accounted for ethically and scientifically as a product that is safe, high quality, and
has efficacy. This is the task of the BPOM in overseeing the efficacy and safety of
drugs before and after distribution," she said.
She said she hoped the public would play an active role by becoming wise in
responding to information related to COVID-19, especially from social media
platforms.
“Let us not easily fall for information that comes from sources that cannot be
accounted for,” she cautioned. (INE)
