Description : In this 60-min presentation, the speaker will guide you through the details of how to identify and use big data for your maximum benefits applicable to FDA-regulated industry.At the end of this seminar, you will learn how to develop and implement best practices to systematically use big data using a CAC-SI method.CAC-SI in this case refers to a Current, Accurate, and Comprehensive strategy in a Systematic, Integrated Manner.Areas Covered in the Session :Applicable Laws, Regulations, Guidance, Rules, StandardsDefinitionsBig Data Sources in Pharmaceuticals and Medical DevicesPower of Big DataData MiningDrug Safety Data and SignalsMedical Device Safety DataSolving Big Problems Using Big DataScience Using Big DataBig Data, Security and Privacy MattersBig Data v. Drug DiscoveryRevolution in FDA-Regulated Industry Using Big DataCompany’s Views on Big DataBig Data: Current TrendsBig Data Driven MedicinesBig Data: Legal, Ethical and Policy IssuesFailure to Use Big DataInadequate Use of Big DataBig Data ManagementBig Data:  OpportunitiesBig Data: ChallengesPost-marketing surveillanceSystematic Use of Big Data: Best PracticesSpeaker’s PASS-IT Suggestions/RecommendationsSpeaker’s Experience and Actual CasesConclusion Who Will Benefit:Regulatory AffairsResearch and Development (Engineers and Scientists)Product Development (Engineers and Scientists)Clinical AffairsQualityMarketingSenior ManagementContractors and subcontractorsConsultantsAnyone interested in the topicPrice tags:LiveSingle Live : For One Participant$ 249Corporate Live : For Max. 10 Participants$ 899RecordingSingle REC : For One Participant - Unlimited Access for 6 Months$ 299For more information and enquiries contact us atCompliance Trainings5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada  Customer Support : #416-915-4458