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.

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.