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ECTD Submission Hanson One day Training Program ID# 14662 April 25 and 26, 2014 Sci tech Center Mumbai, India For more information visit www.diahome.org/IndiaeCTD2014 About The Trainer Saltpeter Berg
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eCTD submission is the electronic Common Technical Document submission process used for submitting regulatory information to health authorities.
Pharmaceutical companies, biotech companies, and medical device manufacturers are required to file eCTD submissions.
eCTD submissions are filled out using specialized software that helps to organize and format the required information according to health authority standards.
The purpose of eCTD submission is to streamline the regulatory submission process, improve data quality, and make it easier for health authorities to review and evaluate submissions.
eCTD submissions typically include information on drug formulation, manufacturing processes, clinical trial data, safety and efficacy information, and labeling.
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