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X-WR-CALDESC:Events for Pharma Journalist
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DTSTART:20160101T000000
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BEGIN:VEVENT
DTSTART;VALUE=DATE:20170906
DTEND;VALUE=DATE:20170908
DTSTAMP:20260515T044257
CREATED:20170502T034747Z
LAST-MODIFIED:20170502T040051Z
UID:1574-1504656000-1504828799@www.pharmajournalist.com
SUMMARY:2nd European Prefilled Syringes Summit
DESCRIPTION:After the success of our first European Prefilled Syringes Summit\, we are pleased to announce the next edition which shall take place on the 6th & 7th September in Berlin\, Germany. \n \nACI’s European Prefilled Syringes Summit will explore the advancements in regulatory guidelines\, product development\, manufacturing processes\, risk mitigation \, portfolio management and answer some infinite industry questions such as; how the industry is responding to disruptive technology\, connectivity\, speed to market\, and next generation syringes. There are several elements that pose a severe challenge to the growth of the global prefilled syringes market\, the primary one being the high costs associated with temperature controlled packaging required for temperature-sensitive drugs. Other more traditional factors inhibiting the market include product recalls due to breakages and leachables\, the potential risk of interaction between prefilled syringes and drugs\, and needle stick prevention. \nKey Topics Include:  \n\nEuropean prefilled syringes market & growth opportunities\nTrends in modern biologics targeting therapeutic classes of drugs that are considered to be the primary growth drivers within the market\nLatest FDA guidelines in receiving PFS & overcoming complex requirements for approval\nSpecialty syringes\, which include prefilled flush syringes\, prefilled diluent systems and contrast agents in prefilled syringe\nConcentrating on Next Generation Smart Devices while Overcoming Traditional Challenges\nManaging the Materials used to Construct Pre-Filled Syringes—Selection and Supply Chain Control\nBalancing biopharmaceutical product portfolio for continual product innovation\, such as incorporating a new delivery component and Creating a lower-risk product development strategy\nUsability: Key Human Factor Attributes & Interactive Considerations.\nThe Drug/Device interface: Integration of the formulation and the device \n\n15% subscriber’s discount available on the registration fee.  \nTo receive the agenda or for the priority registration\, please contact\nMohammad Ahsan on +44 (0)20 3141 0606 or email: mahsan@acieu.net \nConference Fee:               £1\,595 (£240 Discount for all members/subscribers) \nDownload the Brochure : http://www.wplgroup.com/aci/wp-content/uploads/sites/2/2017/03/PPFE2-Agenda_MKT.pdf \nDownload the Brochure Now!
URL:https://www.pharmajournalist.com/event/2nd-european-prefilled-syringes-summit/
LOCATION:Berlin\, Germany\, India
ORGANIZER;CN="Active Communications Europe Ltd (ACI)":MAILTO:mahsan@acieu.net
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170828
DTEND;VALUE=DATE:20170830
DTSTAMP:20260515T044257
CREATED:20170515T091448Z
LAST-MODIFIED:20170515T091721Z
UID:1818-1503878400-1504051199@www.pharmajournalist.com
SUMMARY:7th American Drug Delivery & Formulation Summit
DESCRIPTION:Innovative solutions to the greatest challenges in pharmaceutical development \n\n\nThe growth of biopharma and patient compliance issues have encouraged us to adopt a drug delivery mind set from discovery through to production.Every year we see innovation and breakthroughs at every level of drug development. \nThe DDF Summit brings the most innovative and exciting studies to you. \nCovering both small molecules and biologics\, you’ll find new technologies\, concepts and case studies in areas such as… \n\nFormulation design for poorly soluble compounds\nThe potential of nanotechnology for better deliverability\nThe latest controlled released technologies\nImproving patient compliance by harnessing data and the latest smart device technology\nOptimising formulations for continuous manufacturing\nOvercoming the blood brain barrier and challenges in oral delivery of biologics\nReformulation and biosimilars
URL:https://www.pharmajournalist.com/event/7th-american-drug-delivery-formulation-summit/
LOCATION:The Westin Copley Place Boston Hotel
ORGANIZER;CN="Mark Allen Group":MAILTO:mabconferences@markallengroup.com 
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170809
DTEND;VALUE=DATE:20170810
DTSTAMP:20260515T044257
CREATED:20170515T055826Z
LAST-MODIFIED:20170515T055927Z
UID:1799-1502236800-1502323199@www.pharmajournalist.com
SUMMARY:Pharma CIO Conclave & Awards
DESCRIPTION:Globally\, Indian Pharmaceutical Industry ranks 3rd in terms of volume and is expected to reach US$ 49 Billion by 2020. Over the years\, leading organizations have broken away from the traditional approach and are evolving into a “working with business model”. As Information Technology takes centre stage\, the pharmaceutical industry is trying to leverage technology driven productivity to drive down costs across the value chain. \nThe Pharma CIO Conclave & Awards on the 9 August 2017 in Mumbai will be an ideal platform for your organization to meet\, network & do business with leading C-level decision makers & industry experts within India who are looking for new age technology solutions that can be incorporated within their organization.
URL:https://www.pharmajournalist.com/event/pharma-cio-conclave-awards/
LOCATION:Mumbai\, India
ORGANIZER;CN="Trescon":MAILTO:rajdatta@tresconglobal.com
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170727
DTEND;VALUE=DATE:20170729
DTSTAMP:20260515T044257
CREATED:20170528T235127Z
LAST-MODIFIED:20170528T235409Z
UID:2043-1501113600-1501286399@www.pharmajournalist.com
SUMMARY:International Pharma Regulatory Summit
DESCRIPTION:This event will enable you to effectively interpret complicated regulatory guidelines to fast track your drug approval process \nEarly Confirmed Speakers: \n\nWidyaretna Buenastuti\, Public Affairs & Communications Director\, Pfizer Indonesia\nMay Ng\, Regulatory And Quality Consultant\,Founder\, ARQon Pte Ltd\nShibu Baburaj\, Head\, Regulatory Affairs\, Sanofi-Aventi\nDimas Adityo\, Compliance Director/Head of Ethics & Business Integrity\, Sanofi Indonesia\nRanjodh Gill\, Compilance Manager Quality Assurance\, Parexel\nRakesh Chaurasia\, Head Drug Regulatory Affairs\, PT Dexa Medica\n\nHighlighted features at 2-day conference includes \n\nRegulatory submissions implementation in eCTD format\nThe ASEAN Labelling Harmonisation Effort\nRegistration and approval timeline – combination products and exemptions\nWhat’s new with clinical regulatory requirements in Asia Pacific?\nGlobal trends vs. specific region’s updates for pharmacovigilance\nRegulatory affairs support in providing advices to commercial team for inspection\nGlobal Guidelines for the Development of Biologics \n\nWho Will Attend? \nACI’s summits attract a targeted group of senior level executives with a strict focus on end-users from the industry. \nDirectors/Heads/Managers of Regulatory Affairs\, Quality Control\, Quality Assurance\, Patent/Intellectual Property Rights /Legal\, Pharmacovigilance/Drug Safety \nFor Agenda/Event Brochure\, Information & Registration\, Contact: \nPriyesh Waghmare\n E: pwaghmare@acieu.net | T: +91 (0)20.6527.2803\n Event Website: http://www.wplgroup.com/aci/event/pharma-regulatory-asia/ \nTo request the Latest Agenda & more details on the Programme\, Speakers and their Presentations by email\, please click here>> \n(Quote discount code: PRSf1MP15 to claim for 15% discount- For registration please contact Priyesh Waghmare)
URL:https://www.pharmajournalist.com/event/international-pharma-regulatory-summit/
LOCATION:Singapore
ORGANIZER;CN="ACI":MAILTO:rafael@acieu.net
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170724
DTEND;VALUE=DATE:20170726
DTSTAMP:20260515T044257
CREATED:20170602T084617Z
LAST-MODIFIED:20170725T023425Z
UID:2126-1500854400-1501027199@www.pharmajournalist.com
SUMMARY:5th Digital Pharma China
DESCRIPTION:The Digital Pharma China conference returns to Shanghai this July 24-25 at the Shanghai Marriott Hotel City Centre. Over the past 5 years\, ExL Events and our strategic conference partners\, DXY and BizPro International\, have built a stellar reputation for providing life science marketers with the information they need to drive their businesses and brands to success. As an industry\, life science organizations are navigating the challenges involved with modernizing their business models in order to better engage with their rapidly evolving customer base. Led by an expert speaker faculty of senior-level international and Chinese leaders\, this year’s agenda will focus on how to enable end-to-end digitization of your enterprise through commercial transformation and innovation. This conference will provide attendees with a 360-degree view of digital acceleration and transformation to better serve the needs of their customers. \nTo learn more about this event\, and to register online\, visit digitalpharmaseries.com/china.
URL:https://www.pharmajournalist.com/event/5th-digital-pharma-china/
LOCATION:Shanghai Marriott Hotel City Centre
ORGANIZER;CN="ExL Events":MAILTO:digitalpharma@exlevents.com
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170720
DTEND;VALUE=DATE:20170722
DTSTAMP:20260515T044257
CREATED:20170505T003129Z
LAST-MODIFIED:20170505T003937Z
UID:1688-1500508800-1500681599@www.pharmajournalist.com
SUMMARY:International Pharma Supply Chain Confab
DESCRIPTION: IPSCC 2017 (International Pharma Supply Chain Confab 2017)\, the region’s largest pharma specific supply chain gathering will enable attendees to share best practice on creating regionalised supply chains across the continent\, taking into account specific issues such as temperature control\, supply chain security\, regulatory compliance and supplier management. This 2-day conference is the meeting place for life science supply chain heads responsible for growing and managing their company’s supply chains across the continent. \nEvent Agenda: bit.ly/2nrKrEv \nFor more Info & registration\, please contact Rohan on rbaryah@acieu.net or +48 61 646 7022
URL:https://www.pharmajournalist.com/event/international-pharma-supply-chain-confab/
LOCATION:Jakarta\, Indonesia
ORGANIZER;CN="Active Communications Europe Ltd":MAILTO:rbaryah@acieu.net
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170717
DTEND;VALUE=DATE:20170719
DTSTAMP:20260515T044257
CREATED:20170619T040236Z
LAST-MODIFIED:20170624T201225Z
UID:2295-1500249600-1500422399@www.pharmajournalist.com
SUMMARY:2017 Clinical Trial Protocol Optimization & Design Congress
DESCRIPTION:Exl’s 2017 Clinical Trial Protocol Optimization & Design Congress\, taking place on July 17-18\, 2017 in Philadelphia\, will explore the complex relationship protocol design has with clinical trial success. Attendees will discover new techniques\, hear from industry thought leaders and examine case studies on protocol optimization. This event will bring together sites\, pharma companies\, CROs and other stakeholders in the protocol-writing process to discuss how the industry should change their policies and procedures. With topics on inclusion/exclusion\, advisory boards\, training for protocol writers and patient feasibility\, the congress will foster a space the industry can build upon and make changes to improve all aspects of clinical trial design and planning. \nTo learn more about this event\, and to register online\, visit http://bit.ly/2skdTgn
URL:https://www.pharmajournalist.com/event/2017-clinical-trial-protocol-optimization-design-congress/
LOCATION:Sheraton Philadelphia University City Hotel\, 3549 Chestnut Street\, Philadelphia\, PA 19104
ORGANIZER;CN="ExL Events":MAILTO:todonnell@exlevents.com
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170627
DTEND;VALUE=DATE:20170629
DTSTAMP:20260515T044257
CREATED:20170420T045819Z
LAST-MODIFIED:20170430T063505Z
UID:744-1498521600-1498694399@www.pharmajournalist.com
SUMMARY:Outsourcing in Clinical Trials Medical Devices 2017
DESCRIPTION:OCT Medical Devices moved to Irvine\, California for the first year in 2016\, and we are pleased to say it proved a resounding success. As the only event to cater for the Southern California Medical device hub in Irvine\, it brought together a variety of medical device companies of all sizes\, including Medtronic\, Edwards Lifesciences\, Onciomed\, Inc and St Jude Medical. \n \nThe encompassing agenda focussed on the most pressing topics within the industry\, from emerging markets to medical device reimbursement\, and it still stands as one of the leading clinical focussed events which encompasses discussions across the med-device industry. \nWe are pleased to announce the event will continue its tour of the American medical device hubs\, and for 2017 it will take place in the Santa Clara area within Northern California. \nBased on the success of Irvine\, make sure you don’t miss out on your chance to participate in this event for the first time in Northern California.
URL:https://www.pharmajournalist.com/event/outsourcing-clinical-trials-medical-devices-2017/
LOCATION:Santa Clara\, CA
ORGANIZER;CN="Arena International":MAILTO:events@arena-international.com 
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170607
DTEND;VALUE=DATE:20170609
DTSTAMP:20260515T044257
CREATED:20170420T022117Z
LAST-MODIFIED:20170424T003505Z
UID:732-1496793600-1496966399@www.pharmajournalist.com
SUMMARY:Clinical Trial Supply Nordics Conference 2017
DESCRIPTION:As we enter into 2017\, various changes in the industry have altered the landscape for clinical trial supply businesses.  With this in mind\, our team has developed an extensive and informative agenda to ensure you leave with various concepts to improve your clinical trial supply chain in the ever changing environment. \nEffective forecasting\, risks of temperature deviation and annex 16 are just some of the latest challenges which many clinical trial supply businesses are facing today; the consequences which can occur due to ineffective strategies can lead to start up delays\, stock outs and most importantly rise in costs. At this year’s event\, we aim to embark upon these implications and many more to provide all our attendees with valuable insight into innovative strategies to raise the performance of your clinical trial supply operations. \nKey Speakers at this year’s event: \n\nAnnette Bested Toft\, Director Clinical Trial Supply Management\, Ascendis Pharma (Denmark)\nJonas Fransson\, Director\, Swedish Orphan Biovitrum AB (Sweden)\nDan Markusson\, Chief Operating Officer\, Peptonic Medical AB (Sweden)\nBritta Smedegaard Andersen\, Project Director\, NEXT (Denmark)
URL:https://www.pharmajournalist.com/event/clinical-trial-supply-nordics-conference-2017/
LOCATION:Copenhagen\, Denmark (Venue TBC)
ORGANIZER;CN="Arena International":MAILTO:events@arena-international.com
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170524
DTEND;VALUE=DATE:20170526
DTSTAMP:20260515T044257
CREATED:20170420T015439Z
LAST-MODIFIED:20170424T003536Z
UID:723-1495584000-1495756799@www.pharmajournalist.com
SUMMARY:Clinical Trial Supply West Coast Conference 2017
DESCRIPTION:Clinical Trial Supply West Coast returns in 2017 this time in Burlingame. Attracting the leading biotech and pharma companies from Northern California and beyond\, the event will focus on how drug companies can adapt their supply chains to fit into the highly regulated world. For the first time key topics will be explored through Debates\, Workshops and extended Roundtable discussions. With standout presenters from Sanofi\, Genentech\, Dynavax and Gilead\, this is an event not to miss out on – reserve your place today! \nKey topics in 2017:  \n\nAnnex 16 – Discussion of changes and key strategies to address the sterner QP requirements and their impact on releasing IMP in Europe\nGMP Compliance in Multi-Use Facilities; Defining strategies to maximise usage from pilot GMP facilities\nDetermining the main challenges of shipping clinical supplies into Asia to determine how sponsor companies can prepare adequately for this area\nUnderstanding how best to work with your manufacturers to ensure the efficient production of clinical supplies\nDebate; Breaking it down; Learning how to keep your global clinical supply chain agile and adaptable to regulatory changes
URL:https://www.pharmajournalist.com/event/clinical-trial-supply-west-coast-conference-2017/
LOCATION:Cary\, North Carolina (Venue TBC)
ORGANIZER;CN="Arena International":MAILTO:events@arena-international.com
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170523
DTEND;VALUE=DATE:20170525
DTSTAMP:20260515T044257
CREATED:20170424T235144Z
LAST-MODIFIED:20170424T235222Z
UID:864-1495497600-1495670399@www.pharmajournalist.com
SUMMARY:Outsourcing in Clinical Trials East Coast 2017
DESCRIPTION:This fast-growing event brings together the clinical operations and outsourcing community from the Pennsylvania\, New Jersey\, New York pharma\, biotech and medical device regions and beyond. \nArena International is pleased to announce the return of the Outsourcing in Clinical Trials East Coast conference for its 8th year. The conference will be convening 23-24 May 2017 in King of Prussia\, PA for two days of thought-provoking content which will help you solve your most pressing clinical trial concerns. \nYou will have the opportunity to attend interactive panel discussions and roundtables as well as in-depth case study presentations to discover how you can effectively optimise your clinical outsourcing strategies\, build valuable long-term partnerships and also improve the efficiency of your vendor oversight. \nSpecial features include a medical device specific track on 24th May and a keynote presentation from Ken Getz. \nJoin us for an engaging and informative two days in May by registering your place today and quote MK-PJ!
URL:https://www.pharmajournalist.com/event/outsourcing-clinical-trials-east-coast-2017/
LOCATION:King of Prussia\, Pennsylvania
ORGANIZER;CN="Arena International":MAILTO:events@arena-international.com
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170516
DTEND;VALUE=DATE:20170518
DTSTAMP:20260515T044257
CREATED:20170426T013447Z
LAST-MODIFIED:20170426T014040Z
UID:936-1494892800-1495065599@www.pharmajournalist.com
SUMMARY:Outsourcing in Clinical Trials Europe 2017
DESCRIPTION:Outsourcing in Clinical Trials Europe will take place in Barcelona on the 16th – 17th May 2017 and will bring together Europe’s clinical trial community\, providing the perfect platform for senior-level pharmaceutical and biotech companies to meet with international vendors to build relationships. Returning for its 4th consecutive year\, this flagship conference promises to provide extensive networking opportunities\, interactive presentations and dynamic case studies over two full days. \nProviding more content than ever before\, the agenda is the most exciting yet\, with cutting edge content that will keep you at the forefront of developments in the clinical outsourcing sector for the year ahead and beyond. \nKey sessions include: \n\nLive debate: Considering the influence Brexit will have on European companies\nCase study: Investigating the preferred provider model to identify its reliability\nExclusive presentation: Analysing amendments to GCP and highlighting best practices to ensure your clinical trial is of highest quality\nPanel discussion: Revealing trial advantages experiences through creating a patient centric strategy\nSpeaker hosted roundtable: GCP compliance – how to get prepared as a smaller sponsor company to meet regulators expectations\n\nIf you would like to participate in the above sessions and hear from high profile industry experts\, simply visit the registration page and quote reference code MK-PJ on your booking form to secure one our remaining passes today \nThe OCT team look forward to welcoming you to Barcelona in May for OCT Europe 2017!
URL:https://www.pharmajournalist.com/event/outsourcing-clinical-trials-europe-2017/
LOCATION:Barcelona\, Spain
ORGANIZER;CN="Arena International":MAILTO:events@arena-international.com
END:VEVENT
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