January 17, 2019In the increasingly complex environments of product development lifecycle from clinical phase to registration, commercialization and maintenance, Life Science industry leaders are looking to streamline cross functional business processes and strengthen data governance. This webinar examines practical implications and benefits in creating unified strategic capabilities.
January 21 - 22, 2019 | Beijing, China | Booth #14Asia Pharma R&D Leaders Conference is designed to be a premium strategic platform for big pharmas, biotechs, academia and other stake holders in pharma industry to meet, communicate and establish partnership on pharma R&D.
January 28 - 30, 2019 | Washington, D.C., USDIA's Pharmacovigilance and Risk Management Strategies Conference provides the strongest context, background, updates, new developments, and future direction for regulations and guidance on safety, pharmacovigilance, and risk management strategies that cannot be found in any other meeting.
February 05-07, 2019 | Vienna, AustriaDIA Europe is more than a traditional meeting. It's a chance to learn, engage, and grow as a healthcare professional alongside thousands of cross-functional collaborative leaders.
February 11-13, 2019 | North Bethesda, MD USAt the Regulatory Submissions, Information, and Document Management Forum, DIA will present four tracks and daily health authority plenary sessions to provide a comprehensive view of content and regulatory information management and submissions. All tracks are supported with daily plenary sessions providing regulatory intelligence updates by health authority representatives from FDA, Health Canada, and other regions of interest.
February 18-21, 2019 | Orlando, FL US | Booth #13Celebrating its 10th successful year, SCOPE Summit 2019 provides four stimulating days of in-depth discussions in 19 different conferences, 3 plenary keynote sessions, and the ever-popular interactive breakout discussions. It will focus on advances and innovative solutions in all aspects of clinical trial planning, management and operations, featuring best practice case studies relevant to clinical operations experts.
March 18-20, 2019 | Orlando, FL USDesigned for medical affairs professionals, by medical affairs professionals, this forum provides a comprehensive understanding of the regulatory and compliance environment directly affecting the daily activities of medical affairs and scientific communication professionals.
April 8-10 2019 | Barcelona, Spain | Booth #1
As a valued client, we have an exclusive 25% VIP discount for you. Make sure you use this discount code when you make your booking: CQ5271ARIS
With changes across the regulatory landscape including SPOR, Brexit, and the evolving TMF model, the 2019 eRegulatory Summit includes three jam packed days with the experts to create an industry led conference, which includes tracks on Global eCTD Management, Regulatory Information Management & IDMP Compliance, Trial Master File and a Filing Variations workshop day.
April 15-17 2019 | Philadelphia, PA USEvent is focused on next generation technology, big data, risk and pharmacovigilance, patient centricity and medical devices, and toxicology.
May 20-23 2019 | Beijing, China | Booth #205DIA China is the largest, event in the life sciences industry designed to foster the international exchange of actionable insights to improve health globally through the advancement of lifesaving medicines and technologies in the APAC region.
May 22 - 23, 2019 | London, UK | Booth #8The 5th Annual International Conference and Exhibition in Pharmacovigilance, Regulatory Affairs, Risk Management and Clinical Trials brings together professionals, key decision makers and solution providers from the global pharma industry under one roof for an ultimate knowledge sharing and networking experience.
June 05, 2019 | 10:00 – 11:00AM ESTManaging the drug development lifecycle within pharmacovigilance is challenging. Key stakeholders are under pressure to increase quality, improve compliance, speed up processing times and reduce costs, all the while managing an increasing number of cases. This webinar discusses how automation can address pharmacovigilance-related challenges, with real-world examples of automation in use cases.
Effective Automated Content Management Strategies for Today’s Successful Medical Information Managers
June 18, 2019 | 10:00 – 11:00AM ESTMedical information professionals work with enormous amounts of content and interact with many stakeholders on a day-to-day basis. Automated content management strategies can allow medical information managers to respond to product queries with accurate and timely information across their organization. Join our webinar to learn more.
June 20, 2019 | 10:00 – 11:00AM ESTHistorically, the Regulatory submission and approval process in the life sciences industry has been very reliant on non-standardized documents. Within the last few years, however, regulators have increasingly focused on the submission of structured data and compliance with SPL, xEVMPD, IDMP and UDI standards. This webinar will examine the practicalities, challenges and benefits of structured authoring, and provide some use case examples in the Regulatory space.
June 23 - 27, 2019 | San Diego, CA USDIA's Global Annual Meeting gathers stakeholders from across the world to openly knowledge share, generating insights beyond boundaries to advance innovation in healthcare product development and lifecycle management globally.
October 01 - 03, 2019 | Miami, FL US
The ArisGlobal Life Sciences Technology Summit will highlight how automation can drive transformation and improve efficiency within your organization. It will focus on how a unified and efficient end-to-end product usability strategy increases accuracy and decreases delays for key stakeholders in the drug development process. Attendance at the event is also an opportunity to engage with industry peers to discuss new opportunities to reduce TCO, enable better decision making, and improve productivity.