Do you know that it takes 10 years for a drug to reach to a patient from its initial 
discovery and the average cost for each successful drug to complete this journey is 
$2.6 billion Clinical trials are time consuming and costly. The biggest challenge for 
life sciences organizations has been to reduce drug development costs and cycle time 
and manage diverse data standards and output templates. As organizations are looking 
to streamline data from collection to submission, they envisage an automated and integrated 
metadata driven end to end solution leveraging standards as the driving force. 
But what are the challenges faced in streamlining data? First organizations find managing 
standards and statistical output templates and transforming data to submission ready formats 
extremely difficult. Second, they are seeing limited business and scientific standards and 
content management has study level across different products and therapeutic areas. Lastly, 
absence of a robust governance model to handle and maintain evolving standards and versions 
hamper cross departmental data lineage and oversight. 
TCS AD metadata repository is the answer to these challenges. 
It is a ready to use interoperable metadata driven AI platform 
to manage clinical standards for industry and sponsors. TCS ADD metadata 
repository is comprised of clinical standards, registry and smart governance. 
Automated study build Integrated Metrics and Oversight and Statistical Computing 
and Auto SDTM. It automates all processes from protocol data collection to submission with 
TCS ADD metadata repository platform. Life sciences organizations can achieve up to 30% cost 
reduction in EDC study build efforts up to three to six weeks time reduction in EDC study 
build efforts up to 70% reduction in SDTM efforts. And improved data quality and accelerated compliance. 
Schedule a demo today to understand how TCS ADD metadata repository can streamline your clinical data and 
provide you with superior business outcomes.