ArisGlobal Events

February

| TradeShow

DIA Regulatory Submissions Information and Document Management Forum

February 8, 2021

At the Regulatory Submissions, Information, and Document Management Forum, content and  regulatory information management and submissions. Daily plenary sessions providing regulatory intelligence updates by health authority representatives from FDA, Health Canada, and other regions of interest. 

| Webinar

World Safety US Webinar

February 23, 2021

World Drug Safety Congress US Webinar. Watch live or on demand. Topic overview: Decreasing budgets and increasing case volumes require a more efficient model in drug safety. Is automation part of that model? A recent survey conducted by a global consultancy found that workflow automation is rated as the most critical buying factor when large biopharmas are choosing safety software. Despite the many bold claims around automation in the industry, few have any real-world proof points to support them. 

March

| Webinar

World Drug Safety Congress EU Webinar

March 10, 2021

World Drug Safety Congress EU Webinar. Watch the live webinar or on demand.

| Tradeshow/Webinar

DIA Europe 2021

March 15 – 19, 2021

20 min. Webinar engaging with DIA Europe audience members. DIA Europe 2021 is unique in presenting the entire healthcare value chain ranging from policy and regulations to R&D, marketing and access. Program sessions include topics from nine core thought leadership streams focused on specific therapy areas, including: Beating Cancer, Crisis Preparedness and Response, Smart Health and many more.

| Tradeshow

DIA Medical Affairs and Scientific Communications Forum

March 22, 2021

DIA’s Medical Affairs and Scientific Communications Forum is designed for medical affairs professionals, by medical affairs professionals, regulatory and compliance environment directly affecting the daily activities of medical affairs and scientific communication professionals. 

April

| Tradeshow/Webinar

Global Pharmaceutical Regulatory Affairs

April 20-22, 2021

Comprised of IDMP/SPOR task force members and leading experts in the pharmaceutical field, the Global Pharmaceutical Regulatory Affairs Summit 2021 virtual agenda covers a wide spectrum of the global pharmaceutical regulatory affairs industry. As a virtual attendee, you’ll still be able to interact directly with every speaker to ask questions and uncover solutions to your current challenges.

May

| Webinar

Proventa International Roundtable Webinars

May 11, 2021

Small exclusive Safety executive leaders who face strategic challenges are brought together in this rountable 60-minute webinar discussions. Enables participants to share ideas and lessons learned. Facilitated by ArisGlobal thought leaders, these sessions provide a valuable dialogue over challenges and topical issues. Each roundtable discussion group has a mix of CxO, VP and Director-level individuals which ensures each delegate is given ample opportunity to raise questions and contribute from a strategic perspective.

| Webinar

Transitioning from Medical Information to Medical Intelligence

May 19, 2021

In “Transitioning from Medical Information to Medical Intelligence”, Sandeep Mahagaonkar, Sr. Director, Medical Affairs and Quality Product Management at ArisGlobal, shares his knowledge and expertise on the trends shaping the MI automation space and how medical information teams can be better equipped with new and emerging technologies in business process automation.

| Webinar

IDMP, Key Engine to a Regulatory Strategy

May 20, 2021 at 11:00am EST

Regulatory Departments at EU life science companies are finally gearing up for IDMP implementation after years of policy development. IDMP can be considered a framework for investing in the processes and technology to not only achieve compliance, but to also address the end-to-end processes throughout the regulatory lifecycle. Thinking about IDMP from the beginning of your team’s process will avoid costly delays and achieve full compliance that is also scalable and ready for future growth. IDMP compliance is a timely springboard to address your larger regulatory strategy. We’ll also discuss what investments are needed as we look forward to the future of automation and AI improvements that help simplify compliance processes and bring a new level of innovation to geographically diverse regulatory teams.Please join us on May 20.

| Webinar

Decentralized Clinical Trials – Collaboration Urgency Grows

May 25, 2021 at 11:00am EST

When Covid-19 hit, the concept of decentralized trials suddenly switched from nice idea to necessity. The urgency of the pandemic pushed decentralization to center stage.

During this panel discussion with a case study and Q&A, we will consider:

  • What percentage of current trials are decentralized?
  • How has decentralization changed the nature of collaboration among clinical research partners?
  • What are your primary concerns about putting decentralized trials into operation?
  • How will regulatory authorities respond if more studies add decentralized features?

June

| Tradeshow/Webinar

DIA Annual Global 2021

June 28, 2021

DIA’s virtual 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.

July

| Webinar

Proventa International Clinical Roundtable Webinars

July 20, 2021

Small exclusive Clinical executive leaders who face strategic challenges are brought together in this roundtable 60-minute webinar discussions. Enables participants to share ideas and lessons learned. Facilitated by ArisGlobal thought leaders, these sessions provide a valuable dialogue over challenges and topical issues. Each roundtable discussion group has a mix of CxO, VP and Director-level individuals which ensures each delegate is given ample opportunity to raise questions and contribute from a strategic perspective.

August

| Webinar

R&G PharmaStudies Webinar

August 18, 2021

China’s GVP was recently announced and once implemented on December 1st this year, there will be more stringent and specific requirements for post-market safety monitoring. There are multiple modes of post-market safety monitoring, such as the traditional clinical trial-oriented mode, supplementary trials required by CDE, large-scale epidemiological investigations, specially designed IIT and its combination, retrospective research featuring big data, etc., They are inseparable from the pharmacovigilance system.

Webinar Date and Time: August 18, 2021 at 9:30 am China Standard Time

September

| Virtual Event

RAPS Convergence 2021 | RAPS – Virtual Exibition and Speaker Slot

September 12 – 15, 2021

RAPS Convergence is the largest and most well-recognized annual gathering of regulatory professionals, scientists, and innovators in the world. Convergence brings together representatives from industry, global regulatory bodies, and research, academic and clinical organizations that are directly involved in managing the regulatory process and aligning science, regulation, and business strategy.

Convergence is designed to educate and empower professionals about the ever-evolving healthcare product regulatory environment within an interactive forum that facilitates community exchange, connections and knowledge sharing.

| Virtual Event

Breakthrough2021

September 21 – 22, 2021 – Watch Now On-Demand

ArisGlobal’s Breakthrough2021 is a virtual event that gathers key members of the life sciences and digital health community to provide insights into innovation, AI and digital transformation. This year’s event will feature sessions and keynotes by leading voices from across the industry, aimed at sharing ideas, experiences, and best practices.

Highlights:

  • Listen to leading voices in life sciences across two days of thought-provoking conversations
  • Learn directly from ArisGlobal customers and product leaders as they share R&D technology best practices and successes
  • Access an on-demand library of exclusive, industry-specific content
  • Complimentary attendance for members of the life sciences industry

October

| Tradeshow

Word Drug Safety Congress Europe 2021

October 6 – 7, 2021

Europe’s Most Exciting Drug Safety & PV EventThe World Drug Safety Congress Europe will bring together 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. Join us in Amsterdam.

Location: Amsterdam, Netherlands

Hilton Amsterdam: Apollolaan 138, 1077 BG Amsterdam, Netherlands

Phone: +31 20 710 6000

| Tradeshow

Word Drug Safety US 2021

October 20 – 21, 2021

The World Drug Safety Congress Americas will bring together 600+ top leaders and stakeholders in biopharma to discuss the key challenges they are facing in pharmacovigilance and device safety. Explore strategies in data management & signal detection, showcase how AI & machine learning have improved PV processes, discuss the challenges creating a PV strategy for advanced therapies, and collaborate on medical device safety strategies. This conference is the largest commercial gathering of PV professionals in the world.

Location: Boston, MA

Westin Boston Seaport District: 425 Summer St, Boston, MA 02210

Phone: (617) 532-4600

Hotel: To be booked by ArisGlobal travel desk. Booking link: https://book.passkey.com/e/50172363

| Tradeshow

TMF Summit

October 25 – 27, 2021

The Trial Master File Summit has been the cornerstone event in Clinical Document Management since its inception 10 years ago.

This year’s conference program is guided by our esteemed advisory board and will continue upon its legacy of providing the TMF community with actionable strategies and useful tools needed to return to work informed, equipped, and inspired to guide their organization’s TMF to its full potential! Join our TMF community to experience the education, collaboration, and networking that can only be experienced at the Summit!

Location: New Orleans

November

| Tradeshow

Proventa Clinical Ops East Coast

November 2, 2021

Tired of the same conference experience? Real discussions and genuine networking are often promised, but not always delivered.

Proventa International’s Clinical Strategy Meetings are designed to avoid the pitfalls of a typical conference, by providing the right environment to make those important connections through interactive roundtable discussions, exclusive networking and keynote panel debates. Join Clinical Operations professionals from across the West Coast in San Francisco, to discover new insights and take your company’s mission to the next level.

| Tradeshow

Proventa Clinical Ops West Coast

November 17, 2021

Tired of the same conference experience? Real discussions and genuine networking are often promised, but not always delivered.

Proventa International’s Clinical Strategy Meetings are designed to avoid the pitfalls of a typical conference, by providing the right environment to make those important connections through interactive roundtable discussions, exclusive networking and keynote panel debates. Join Clinical Operations professionals from across the West Coast in San Francisco, to discover new insights and take your company’s mission to the next level.

| Tradeshow

Pharmacovigilance World 2021 | Pharmaceutical Conference

November 23 – 24, 2021

Online | Conference, Expo and Workshop

Register and join our session on Day 1: Pivoting Safety to a Strategic Center – with an End-to-end AI Enabled Data Fabric

  • Learn how technology and industry trends are creating opportunity to transform safety to a strategic driver.

  • Gain perspective on how safety systems must evolve to seize this opportunity.

  • Hear about ArisGlobal’s progress toward enabling the future of pharmacovigilance.

December

| Tradeshow

Proventa Clinical Ops East Coast

November 2, 2021

Tired of the same conference experience? Real discussions and genuine networking are often promised, but not always delivered.

Proventa International’s Clinical Strategy Meetings are designed to avoid the pitfalls of a typical conference, by providing the right environment to make those important connections through interactive roundtable discussions, exclusive networking and keynote panel debates. Join Clinical Operations professionals from across the West Coast in San Francisco, to discover new insights and take your company’s mission to the next level.

| Tradeshow

Proventa Clinical Ops West Coast

November 17, 2021

Tired of the same conference experience? Real discussions and genuine networking are often promised, but not always delivered.

Proventa International’s Clinical Strategy Meetings are designed to avoid the pitfalls of a typical conference, by providing the right environment to make those important connections through interactive roundtable discussions, exclusive networking and keynote panel debates. Join Clinical Operations professionals from across the West Coast in San Francisco, to discover new insights and take your company’s mission to the next level.

| Webinar

Beyond Compliance: Preparing for IDMP now and into the Future

December 8th, 2021

Online | 30 Minute Video Presentation | 10 Minutes of Live Audio Q&A

IDMP data standards are forcing companies to capture more data than ever before – and effective data management can be time-consuming and costly. With the right technology and processes in place, organizations can get ahead of changing regulations and timelines, increasing their compliance agility, and minimizing expenditure risks.

Join this webinar to learn:

  • Best practices for collecting, extracting, and enriching your data for submission

  • How to increase cross-departmental business process efficiency

  • Ways to support your journey through continued xEVMPD compliance, multiple phases of IDMP compliance, UDI and beyond

 

The time is now to make sure your organization is prepared.