The multinational corporation selected INFOTEHNA after an intensive evaluation of 11 vendors, and opted for two of INFOTEHNA’s solution modules, RIMExpertTM and SubmissionExpertTM, which will be integrated into the company’s existing IT landscape. These solutions will help several hundred users worldwide to efficiently manage and track global regulatory submissions, and thus tackle challenges pertinent to the upcoming regulation changes.
The two modules are part of INFOTEHNA’s myPharmaExpertTM solution suite, which boosts the ability of customers worldwide to improve the overall product lifecycle management efforts, reduce time-to-market for new products and introduce sustainable compliance. Being easily configurable and validated, myPharmaExpertTM Suite is capable of supporting either singular compliance relevant processes or complete enterprise compliance management.
“By standardizing our solutions across the organization, employees will have instant access to the most recent information of regulatory submissions lifecycle statuses,” explained Elvis Paćelat, INFOTEHNA’s CEO and euroscript group’s Vice President Life Sciences. “Users will be able to collaborate efficiently in a compliant manner and respond to change rapidly. This will speed up regulatory compliance processes and delivery of quality products, which the company has always been committed to,” he added.