Regulatory Information Management Systems Conference

January, 2020 | Arlington, VA

Regulatory Information Management Systems Conference
January, 2020 | Arlington, VA

Request Invite

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

“I thought the conference was excellent!  Having a conference tailored to one discipline made each panel and contact relevant.”

Director, Compliance & Legal Affairs
Orexigen

“Great insight to hear payer perspective in contracting and account management and the changing healthcare landscape.”

Channel Liaison
Biogen

“It was definitely an excellent well-rounded opportunity to meet new people, get new ideas, and get an in-depth education on what’s to come with the FDA collaborations.”

Quality Engineer
Centurion Medical Products

“It was very well organized event and high quality, the fact to have an IVD track was also interesting. Thanks, I will recommend the Q1 event!”

Regulatory Affairs – EMEA Regional Head
BIOMERIEUX

“The organization and support staff were fantastic! I’m looking forward to next year.”

Global Business Project Lead
Genentech

About the Conference:

Across the life sciences industry, pharmaceutical, biotechnology, medical device and diagnostic corporations gather an unprecedented volume of product safety and efficacy evidence to support both initial product approval as well as supporting long-term compliance requirements. Integration and alignment of regulatory information management systems is increasingly allowing globalized corporations the ability to visualize larger data sets, rapidly retrieve information and take advantage of digitization efficiencies. As regulatory authorities and payer stakeholders increasingly demand a greater volume of data with deeper analytic insights, regulatory information systems will play a pivotal role in ensuring supporting data can be efficiently collected, analyzed and deployed.

Core Topics to be Addressed:

  • Establishing a single authoritative source of information
  • Global harmonization & tracking of regulatory documentation
  • Opportunities for improving quality & usability of regulatory data
  • Integration of multiple regulatory technologies into an aligned system

Core Topics to be Addressed:

  • Establishing a single authoritative source of information
  • Global harmonization & tracking of regulatory documentation
  • Opportunities for improving quality & usability of regulatory data
  • Integration of multiple regulatory technologies into an aligned system

Request Invite

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

Audience

75 Attendees

All attendees come directly from life science companies

Distinguished Presenters

Speaker recruitment in process

Networking

Networking time is built into the agenda to allow industry peers to connect and exchange ideas

Open Dialogue and Group Share

Each presentation is followed by 10-15 minutes of open dialogue for questions and exchange of best practices

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