January 30, 2018The 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.
January 16 – 18, 2018 | Orlando, FL, USTrial 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.
January 22 – 24, 2018 | 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 15, 2018DCVMN 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, 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. This Forum provides multiple opportunities for networking, knowledge sharing, and education for both business- and technology-focused attendees.
February 12 – 15, 2018 | Orlando, FL, USSCOPE 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, USDIA’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.
March 21 – 22, 2018 | Rancho Mirage, CA, USThe 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.
April 10 – 11, 2018 | Philadephia, PA, USThe 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.
April 11 – 12, 2018
April 11 – 12, 2018
April 17 – 19, 2018 | Basel, SwitzerlandDIA 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.
April 23 – 26, 2018
April 24 – 26, 2018 | Barcelona, SpainWith 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.
May 9, 2018The 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.
May 22 – 25, 2018 | Beijing, ChinaThe 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.
June 24 – 28, 2018 | Boston, PA, USThe 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.
July 2 – 3, 2018 | London, UKIn 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.
July 3, 2018In 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.
19, July, 2018The Chinese Federal Drug Authority (CFDA) regulations are changing and that brings both challenges and opportunities. This webinar will address latest CFDA regulations announcement and the impact on domestic and global companies and how cognitive technologies can help pharma industry stay E2B R3 compliant.
July 17, 2018On 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.
September 10 – 11, 2018 | Amsterdam, NetherlandsWorld 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.
September 10 – 11, 2018 | Vienna, AustriaThe 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.
September 23 – 26, 2018 | Seattle,WA, USThe 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.
November 11 – 13, 2018 | Tokyo, JapanThe 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, AustriaThe 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.
September 28 – 29, 2018 | Barcelona, SpainPartnership in Clinical Trials will bring the latest information from across the clinical trials spectrum and providing direct access to the industry’s leading innovators.