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DTSTART:20170101T000000
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DTSTART;VALUE=DATE:20181016
DTEND;VALUE=DATE:20181019
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SUMMARY:12th Digital Pharma East
DESCRIPTION:Join more than 800 attendees for the largest event focused exclusively on digital marketing for the life sciences — Digital Pharma East. Our faculty of more than 120 senior-level professionals share their lessons learned and actionable insights to help you leverage innovation to provide an optimal customer experience and improve health outcomes. \n  \nTo learn more about this event\, and to register online\, visit digitalpharmaseries.com/east
URL:https://www.pharmajournalist.com/event/12th-digital-pharma-east/
LOCATION:Pennsylvania Convention Center\, 1101 Arch Street\, Philadelphia\, PA\, 19107\, United States
ORGANIZER;CN="ExL Events":MAILTO:digitalpharma@exlevents.com
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DTSTART;VALUE=DATE:20181017
DTEND;VALUE=DATE:20181019
DTSTAMP:20260515T022853
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SUMMARY:European Drug Safety Summit 2018
DESCRIPTION:ACI’s European Drug Safety Summit 2018 will take place in London on 17th & 18th October. The two day event will bring together pharmacovigilance personnel from key pharmaceutical companies and will address the challenges in monitoring and maintaining drug safety strategies. The event will also discuss how to apply new technologies and strategic approaches to effectively manage drug safety and will discover key developments in the handling\, analysis and reporting of adverse events during trials and understand the regulators requirements with the aim of speeding drugs to market whilst mitigating the risk of recall. \nKey Topics Include: \n\nMeeting Safety Requirement: Regulator’s Perspective\nBuilding a Pharmacovigilance Strategy\nEvolving PV Strategies for Tomorrow\nTechnological Advancement in Pharmacovigilance\nClinical Data Management\nThe Role of Big Data and Social Media in PV\nEnsure Drug Safety & Risk Minimisation Measures\nLatest Development & Innovation Approach for Effective Signal Management\nDevelopment of Qualified Personal Responsible for Pharmacovigilance (QPPV)\nPharmacovigilance for Advanced Therapies\n\nWho Will Attend? \nAttendees will be drawn primarily from pharmaceutical\, biotechnology and contract research organisations and include VPs\, Directors and Managers/Scientists working in Drug Safety\, Pharmacovigilance\, Epidemiology\, Clinical Research and Development\, Clinical Trial Management\, Pharmacology\, Regulatory Affairs and Compliance\, Strategy and Business Development\, Risk Management\, QPPV.
URL:https://www.pharmajournalist.com/event/european-drug-safety-summit-2018/
LOCATION:London\, UK
ORGANIZER;CN="ACI":MAILTO:cwilliams@acieu.net
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DTSTART;VALUE=DATE:20181017
DTEND;VALUE=DATE:20181019
DTSTAMP:20260515T022853
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SUMMARY:Pharma Cold Chain Summit 2018
DESCRIPTION:ACI’s Pharma Cold Chain Summit 2018 will be taking place on the 17th & 18th October in London\, UK. The two day event will bring together leading experts and stakeholders from across the sector for two days of engaging presentations and interactive discussions. The core challenges and critical issues will be tackled to maintain a robust Cold Chain Management across the global Pharmaceutical Supply Chain. \nJoin us for a balanced programme of practical\, commercial\, case-study-based discussions\, and to meet industry thought leaders and senior-level decision-makers in an informal environment ideal for sharing ideas and making new contacts. \nAgenda: http://bit.ly/2D3csY7
URL:https://www.pharmajournalist.com/event/pharma-cold-chain-summit-2018/
LOCATION:Virtual Conference: Online Access Only
ORGANIZER;CN="Active Communications International%2C Europe":MAILTO:rbaryah@acieu.net
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DTSTART;VALUE=DATE:20181017
DTEND;VALUE=DATE:20181019
DTSTAMP:20260515T022853
CREATED:20180511T115222Z
LAST-MODIFIED:20180511T115339Z
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SUMMARY:Orphan Drugs and Rare Diseases Conference
DESCRIPTION:This year’s SMi’s Orphan Drugs and Rare Diseases Conference will bring together regulatory agencies\, pharmaceutical companies\, non-profit organisations and orphan drugs developers to construct an agenda that addresses the driving economic factors\, policies and issues that will affect the development of orphan drugs globally including commercialization\, policies\, reimbursement\, and pricing. \nKeep up to date with the industry and to learn from expert speaker panel\, bringing you important new case studies and reports on this year’s relevant topics. \n\nHIGHLIGHTS IN 2018: \n\nDiscuss the pricing and reimbursement of orphan drugs\nUnderstand the challenges of patient recruitment and patient-centric research\nHear the MHRA’s perspective on benefit-risk assessment in rare diseases\nExplore the clinical development of orphan drugs for rare disease\nGain insight into potential synergies between regulators and assessors\n\nSPEAKERS INCLUDE: \n\nCarina Schey\, Researcher\, University of Groningen\nSheela Upadhyaya\, Associate Director\, Highly Specialised Technologies\, National Institute for Health and Care Excellence (NICE)\nXavier Ortega\, Project Manager\, Rare Diseases\, Minoryx\nNigel Nicholls\, Director and Country Manager UK/Ireland\, BioMarin Europe Ltd\nYolanda Barbachano\, Senior Statistical Assessor\, MHRA\nMichale Bouskila-Chubb\, Head of Business Development\, Healx\n\nView detailed agenda\, find out who is speaking and book to attend at http://www.orphandrugs.co.uk/phjWL \nTwitter – @SMIpharm & #smiorphandrugs\nLinkedIn – SMi Pharma\nOpt-in – SMi Group value your interest in their events and would like to stay in touch – opt-in via https://www.smi-online.co.uk/opt-in to receive SMi’s updates
URL:https://www.pharmajournalist.com/event/orphan-drugs-and-rare-diseases-conference/
LOCATION:Holiday Inn Kensington Forum\, London\, United Kingdom
ORGANIZER;CN="SMi Group Ltd":MAILTO:ldurneva@smi-online.co.uk
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