ArisGlobal Events

2018 Events



DIA Webcast: Re-Think Your Integrated CTMS

January 30, 2018

The adoption of modern, unified drug development platforms would eliminate the bigger operational issues and increases the possibilities to leverage cloud and newer technologies like cognitive computing. View this webcast and learn how unified solutions in clinical trials efficiently streamlines trial management process.

Trial Master File Summit

January 16 – 18, 2018 | Orlando, FL, US

Trial Master File Summit is the premier educational event for CROs, sponsors and sites to share best practices for TMF filing both in electronic and paper format. ArisGlobal will be part of this event showcasing the best in class clinical solutions for trial management and EDC.
Speaker slot

DIA PV & Risk Management Strategies

January 22 – 24, 2018 | 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.



DCVMN members only

February 15, 2018

DCVMN is a voluntary public health driven alliance of vaccine manufactures from developing countries with an objective to strive for an International recognition such that developing country vaccine manufactures have an essential role in assuring the availability of quality vaccines for national immunization programs


February 5 – 7, 2018 | 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. This Forum provides multiple opportunities for networking, knowledge sharing, and education for both business- and technology-focused attendees.


February 12 – 15, 2018 | Orlando, FL, US

SCOPE Summit offers plenary conferences and sessions, focused on advances and innovative solutions in all aspects of clinical trial management and operations, including Site Selection and Management, Patient Engagement, Recruitment and Retention, Project Management, Outsourcing, Forecasting, Budgeting and Contracting, Risk-Based Monitoring and Clinical Supply Management.




March 19 – 21, 2018 | Rancho Mirage, CA, US

DIA’s Medical Affairs and Scientific Communications Forum is 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.

MI Tech Forum

March 21 – 22, 2018 | Rancho Mirage, CA, US

The main goal of MI-TECH is to facilitate a medical information industry collaboration in order to address the most pressing and important technology concerns. The event will examine the newest trends in technology being utilized throughout the medical information industry and how the industry can benefit from these advancements.



WDS Congress Americas

April 10 – 11, 2018 | Philadephia, PA, US

The World Drug Safety Congress Americas is thrilled to introduce new sessions on technologies ranging from AI, automation and combinational products to social media safety signal detection, structured benefit-risk assessments and novel methods of reporting. With over 20 global pharmaceutical heads in PV speaking on the program, the 2018 conference is set to be bigger and better than ever before.
ArisGlobal Meeting

ArisGlobal Regulatory Advisory Board

April 11 – 12, 2018

ArisGlobal Meeting

ArisGlobal Safety Advisory Board

April 11 – 12, 2018


DIA Euro Meeting

April 17 – 19, 2018 | Basel, Switzerland

DIA is a global association that mobilizes life science professionals from across all areas of expertise to engage with patients, peers and thought leaders in a neutral environment on the issues of today and the possibilities for tomorrow. The 2018 DIA Euro Meeting will focus on an increased collaboration between the regulatory and the HTA/ payer environment.
ArisGlobal Meeting

Safety ISP Workshop

April 23 – 26, 2018


eReguatory Summit

April 24 – 26, 2018 | Barcelona, Spain

With changes across the regulatory landscape including SPOR, Brexit, and the evolving TMF model, the 2018 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.



DIA Webcast: PV & Automation Use Cases

May 9, 2018

The regulatory and pharmacovigilance landscape is evolving substantially with the changing expectations from regulatory authorities. View this webinar to learn how cognitive computing technologies can automate a multitude of tasks in pharmacovigilance and regulatory, including productivity, compliance, and data quality.

DIA China

May 22 – 25, 2018 | Beijing, China

The 10th DIA China Annual Meeting will bring together pharmaceutical R&D professionals from different continents and regions, involved at all levels of the health care product development spectrum, to discuss recent and upcoming transformational changes for China’s innovation and regulatory environments.



DIA Annual

June 24 – 28, 2018 | Boston, PA, US

The DIA 2018 Global Annual Meeting brings together thousands of innovators from around the globe. The event is designed to foster the international exchange of actionable insights to improve health globally through the advancement of lifesaving medicines and technologies.



Regulatory Affairs for Medical Devices

July 2 – 3, 2018 | London, UK

In this digital age, we are experiencing an overload of information. Regulatory Affairs for Medical Devices (RAMD 2018) will filter through this overload to deliver targeted information and streamline the regulatory process to ensure a smooth and successful introduction in the Medical Device Market.

From Push to Pull with EMA: A Modern Take on Triaging Adverse Events

July 03, 2018

In October 2017, the European Medicines Agency (EMA) changed the way in which they deliver safety information to Marketing Authorisation Holders by leveraging E2BR3 format. The webinar will discuss on the changes to safety information handling by the EMA and how machine learning can be used to add efficiency and automate the search for relevant cases.

Practical Implementation of GDPR within Medical Information

July 17, 2018

On May 25, 2018 the long awaited Global Data Privacy Regulation (GDPR) was implemented. For breaking the law, companies will pay up to 4% of their global revenues or €20 million, whichever is greater. Join this webinar to understand how to address practical implementation of GDPR within a medical information system.



ICH Regulation and Compliance in China: Get ready Today for Tomorrow

August 01, 2018

When it comes to ICH regulations, China is in an exciting phase of change. Organizations must be in compliance with the regulations by 2019, and knowing whether your current provider gives you what you need should be assessed immediately. This webinar will address the lasts ICH regulation and compliance and discuss the potential impact of these regulations both now & 2019.

The Evolution of CNDA Regulations: Get Ready for 2019 Compliance

August 30, 2018

On July 27, the Chinese National Drug Administration (CNDA) released supplemental guidance (No. 50) on IND clinical trial procedure that brings both challenges and opportunities. This webinar addresses the impact on domestic and global companies and explores what is required to be compliant with the latest regulations.



WDS Congress Europe

September 10 – 11, 2018 | Amsterdam, Netherlands

World Drug Safety Congress Europe was the first strategic pharmacovigilance event to unite a plethora of stakeholders in drug safety, from pharma and biotechs to regulators and patients. The event continues to lead the way in moving the sector for its ability to connect key stakeholders.
Speaker slot

Risk Management & Pharmacovigilance Summit

September 10 – 11, 2018 | Vienna, Austria

The 5th Annual Risk Management and Pharmacovigilance Summit will focus to create great atmosphere for PV professionals to network and discuss current issues in the drug safety world.

SCDM 2018 Annual Conference

September 23 – 26, 2018 | Seattle,WA, US

The SCDM Annual Conference is an unforgettable professional experience, offering unrivalled opportunities to discover cutting-edge solutions and best practices in the Clinical Data Management industry.


ArisGlobal Meeting

ArisGlobal Life Sciences Technology Summit

October 2 – 3, 2018

The 2018 ArisGlobal Life Sciences Technology Summit is the annual event that brings together our customers from Pharmacovigilance and Safety, Regulatory, Clinical Development, and Medical Affairs. Join other life sciences professionals from pharma, biotech, medical devices and contract research organizations to hear about industry news and trends, product updates, and best practices.



DIA Japan 2018

(Booth #5&6)

November 11 – 13, 2018 | Tokyo, Japan

The 15th DIA Japan Annual Meeting 2018 will discuss on innovative technologies such as AI, big data/genomics, and cell/gene therapies which are poised to transform healthcare product development across the globe.

November 14 – 15, 2018 | Vienna, Austria

The 12th Annual European Medical Information and Communications Conference and Exhibition is the only European forum dedicated to medical information and communications, organised by medical information and communications professionals.
Speaker slot

Partnerships in Clinical Trials

November 29, 2018, 10:00AM CEST | Barcelona, Spain

Partnership in Clinical Trials will bring the latest information from across the clinical trials spectrum and providing direct access to the industry’s leading innovators.