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3rd Annual Life Science Regulatory Intelligence & Strategy Conference 

November, 2020 | Arlington, VA

3rd Annual Life Science Regulatory Intelligence & Strategy Conference
November, 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:

Life science organizations must consider a holistic approach to regulatory affairs with a large portion of the process attributed to regulatory intelligence and the collection of all relevant policy information to speed time to market for products and ensure company compliance. Regulatory intelligence teams are responsible for monitoring a multitude of databases, working groups, and industry new outlets to remain abreast of both US requirements as well as developing international policies in regions such as the EU, Asia Pacific, and Latin America. In addition, regulatory intelligence teams are involved in policy to comment on draft guidance and impact future regulations in favor of the industry as well as partnering with strategy teams to implement intelligence into product and organizational planning.

Core Topics to be Addressed:

  • Best practices to collect and filter intelligence with available resources
  • Tracking regulatory trends to predict possible policy & industry updates
  • Effective methods to employ during FDA & global commenting processes
  • Product and organizational strategies based on collected intelligence
  • Techniques to deliver regulatory intelligence to internal stakeholders

Program Highlights:

  • Blend of regulatory perspectives from intelligence, policy & strategy
  • Combination of sessions including workshops, case study & panels
  • Focus on solutions to secure regulatory approval & ensure compliance

Core Topics to be Addressed:

  • Best practices to collect and filter intelligence with available resources
  • Tracking regulatory trends to predict possible policy & industry updates
  • Effective methods to employ during FDA & global commenting processes
  • Product and organizational strategies based on collected intelligence
  • Techniques to deliver regulatory intelligence to internal stakeholders

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 progress

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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