EDM and ERS is combining with RIM in 2015 for the eRegulatory and Intelligence Annual Conference. In recent years, industry as a whole has been converging towards looking at regulatory as an end-to-end process. Document management, publishing and technical regulatory requirements are all subsets of regulatory information management at its broadest definition.
The program committee is developing this conference featuring plenary sessions on latest trends in the industry as well as FDA and other Agency updates for direct dialogue with industry. This conference serves as a forum for the discussion of emerging standards and the processes for submission creation and maximum use of regulatory information.
MakroCare is an international Drug / Device development and consulting services firm operating since 1996. MakroCare has successfully helped many Pharma, Biotech and Device companies’ right from designing their Regulatory Strategy to getting product approvals globally. We have been managing more than 4000 Regulatory submissions (Clinical, Market Authorization and Post Market Maintenance Applications) annually.
MakroCare has developed Multi-Dimensional Regulatory Service Accelerators (NAVAT) that is helping companies to accelerate their Global Submissions and receive faster Approvals. In addition, our functional services include CMC Authoring, Clinical Authoring, LCM, Labeling & Submission Management.
Meet our expert Regulatory team in this conference, to know more about our Services.