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Good Clinical Practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects. Compliance with this standard provides public assurance that the rights, safety, and well-being of trial subjects are protected, consistent with the principles that have their origin in the Declaration of Helsinki, and that the clinical trial data are credible.
Clinical data management (CDM) is a critical process in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials. Clinical data management ensures collection, integration and availability of data at appropriate quality and cost.
Medical writing involves writing scientific documents of different types which include regulatory and research-related documents, disease or drug-related educational and promotional literature, publication articles like journal manuscripts and abstracts, content for healthcare websites, health-related magazines or news articles.
I would like to thank Dr. Maha for the simple explanation of the content that is not simple at all ❤❤❤❤Thank you, Dr. Maha, for information in the courseSomeone said that GCP is more important in manufacturing and corporate research, not just academic research, but if it is also applied in academic...
Dr. Nouran Hamza is a Brand of creativity and professionalism. I've completed attending her biostatistics course using R software (3 modules). It's a powerful course that contains all the information needed to start a data science road. She has helped us with all the information and energy she has....
I strongly recommend Dr. Nouran as an excellent professional biostatistician.
Dr. Nouran is the best instructor I have ever seen. She has all qualification for success
Dr Nouran prepared us to face the real world, she always guides us.