ArisGlobal Events

2019 Events



From Good to Great: The Benefits of a Unified Clinical and Regulatory Data Management Strategy

January 17, 2019

In 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.

9th Asia Pharma R&D Leaders Conference

January 21 - 22, 2019 | Beijing, China | Booth #14

Asia 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.

DIA PV & Risk Management Strategies

January 28 - 30, 2019 | Washington, D.C., US

DIA'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.



DIA Europe

February 05-07, 2019 | Vienna, Austria

DIA 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.

Regulatory Submissions, Information and Document Management (RSIDM)

February 11-13, 2019 | North Bethesda, MD US

At 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 #13

Celebrating 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.



DIA Medical Affairs and Scientific Communications Forum

March 18-20, 2019 | Orlando, FL US

Designed 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.


World Drug Safety Congress Americas 2019

April 15-17 2019 | Philadelphia, PA US

Event is focused on next generation technology, big data, risk and pharmacovigilance, patient centricity and medical devices, and toxicology.



DIA China 11th Annual Meeting 2019

May 20-23 2019 | Beijing, China | Booth #205

DIA 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.

Pharmacovigilance Europe Congress

May 22 - 23, 2019 | London, UK | Booth #8

The 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.



Key Use Cases of Automation in Pharmacovigilance

June 05, 2019 | 10:00 – 11:00AM EST

Managing 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 EST

Medical 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.

Next-Generation Structured Authoring: Seamless Synchronization Between Data and the Document

June 20, 2019 | 10:00 – 11:00AM EST

Historically, 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.

DIA 2019 Global Annual Meeting

June 23 - 27, 2019 | San Diego, CA US

DIA'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.



Building an Automatic-Centric Approach to Drug Safety

July 18, 2019 | The Charles Hotel, Cambridge, MA

Join ArisGlobal at The Charles Hotel in Cambridge, Massachusetts on July 18, 2019 for a complimentary “Lunch and Learn” as Edwin Raj, Senior Director and Head of Safety Operations for AMAG Pharmaceuticals discusses his company’s journey to enhanced PV automation, and his roadmap for future drug safety innovations.



World Drug Safety Congress Europe

September 10-11 2019 | Amsterdam, Netherlands

The World Drug Safety Congress Europe will bring together 550+ drug safety, pharmacovigilance, data analytics, epidemiology, and other key players in the biopharma sector. Explore the use of big data and AI in pharmacovigilance, examine benefit-risk management strategies and patient-centric approaches; discuss how you can tackle the challenges of social media and drug safety legislation globally.



ArisGlobal Life Sciences Technology Summit

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.


Automation in Pharmacovigilance: From Hype to Reality

October 15, 2019 | 10:00 – 11:00AM EST

Throughout the last three years, the life sciences industry has been trying to find a way to make the potential benefits of automation, such as reduced manual intervention in case processing, a reality for their organizations. However, very few organisations have been able to make any significant progress on making this a reality. It is therefore important to identify how biopharmaceutical companies can achieve these benefits both now and in the future, and move away from the hype that surrounds automation.



DIA Japan 16th Annual Meeting 2019

November 10-12 2019 | Tokyo, Japan | Booth #30-32


DIA Medical Information and Communications Conference and Exhibition

Nov 20 - 21, 2019 | Lisbon, Portugal

This is a unique meeting organised by medical information professionals for medical information professionals. The agenda includes key trends in medical information, digital developments and hot topics/challenges attracting decision makers dealing with such issues on a daily basis.