Meet DDiSmart at ACDM Annual Conference 2014, UK

DDi is presenting mEDC and ClinMetanoia at the ACDM Annual Conference that's being held from 9th to 11th March 2014 at De Vere Wokefield Park, Reading, UK.

DDi is presenting mEDC and ClinMetanoia at the ACDM Annual Conference that's being held from 9th to 11th March 2014 at De Vere Wokefield Park, Reading, UK.

mEDC is a web based electronic data capture and clinical data management system designed to support all clinical trial phases from phase I to Late Phase/ Post-Market Surveillance studies during the medical development process. DDi has a successful track record in conducting various clinical trials using mEDC.

ClinMetanoia tool is an innovative clinical intelligence tool used by our clients in various clinical development domains and therapeutic areas to strategize Clinical-IT needs. It facilitates Real-time Data, Risk Based Monitoring, Clinical Analytics and integrated e-Clinical data through a collaborative portal. ClinMetanoia tool uses the clinical trial data from various sources using client's existing technical infrastructure, thus optimizing their e-clinical systems and delivering great results.

DDismart is an e-Clinical and Data integration services company and a prominent partner to provide clinical informatics and IT solutions to the Life Sciences industry.

Visitors/delegates are welcome to visit our booth to learn more about our company, e-clinical products and services.

About DDismart:

DDismart is a prominent partner to provide clinical informatics and IT solutions to the Life Sciences industry. Being an IT subsidiary of MakroCare which is a world-class medical development, consulting and commercialization services company, DDi has built its technology competency with a unique blend of functional and domain expertise to serve the e-clinical needs of its clients across the globe.

DDi caters to the Life Science organizations of varied sizes. Our customer base includes organizations from top 50 pharmaceutical companies to small & mid-size biotechnology, medical device companies and academic/ research institutes. Our products and solutions are completely validated and have been designed to support the requirements of internationally recognized ICH-GCP, HL7, FDA 21 CFR Part 11, HIPAA, GAMP5 and other regulatory standards.

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Tags: clinical research software, clinical trial systems, clinical trials software


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