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Validation Failure: Cause, Avoidance and Recovery

Validation Failure: Cause, Avoidance and Recovery

by Natalie Zunker | Nov 20, 2019 | Medical Device

Natalie Abts, Head of Human Factors Engineering at Genentech is one of the many leading speakers at the upcoming Medical Device Human Factors and Usability Conference.

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Regulatory Intelligence Advances in Technology

Regulatory Intelligence Advances in Technology

by Allison McIlvain | Nov 8, 2019 | Life Science

Disruptive technologies are one of many contributing factors to the changing regulatory intelligence industry.

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The Evolution of Regulatory Intelligence Teams

The Evolution of Regulatory Intelligence Teams

by Allison McIlvain | Oct 28, 2019 | Pharmaceutical

Linda Bowen is presenting at this year’s 2nd Annual Life Science Regulatory Intelligence, Strategy & Execution Conference.

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Navigating Health Authorities in CMC

Navigating Health Authorities in CMC

by Allison McIlvain | Oct 25, 2019 | Pharmaceutical

The 5th Annual Global Regulatory Affairs CMC Conference dives deep into challenges CMC teams are facing and provides networking opportunities to benchmark and workshop with peers.

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Transitioning to e-beam or X-ray

Transitioning to e-beam or X-ray

by Natalie Zunker | Oct 22, 2019 | Medical Device

The 6th Semi-Annual Medical Device Sterilization Conference takes place October 29-30 in Alexandria, VA.

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Medical Information Teams as Strategic Leaders

Medical Information Teams as Strategic Leaders

by Allison McIlvain | Jul 1, 2019 | Speaker Interview

  Maureen Bot, Head Medical Information at Amgen Canada Inc., is one of many experts presenting at this year’s Customer Centric Medical Information Conference taking place this July. Preview topics that the event dives deep into below.   Can you please give...

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FDA Guidance’s Impact on Ad & Promo

FDA Guidance’s Impact on Ad & Promo

by Allison McIlvain | Jun 28, 2019 | Life Science, Speaker Interview

Glenn Byrd, an expert in strategic promotional regulatory affairs, is one of many professionals presenting at this year’s Life Science Advertising & Promotions Regulatory Affairs Conference. Preview some of the many topics featured at this year’s event below....

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Methods for Quantifying Results in Patient Advocacy

Methods for Quantifying Results in Patient Advocacy

by Allison McIlvain | May 29, 2019 | Life Science, Speaker Interview

Michael Bodulow, Senior Specialist, Patient Advocacy at Biomarin Pharmaceutical Inc., and Tara Herington, Vice President at Cardinal Health Sonexus™, are presenting at Q1’s 8th Annual Strengthening Patient Advocacy Engagement Conference this July.

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Enhancing Medical Communication Deliverables

Enhancing Medical Communication Deliverables

by Allison McIlvain | May 15, 2019 | Life Science, Speaker Interview

Elizabeth Pham, PhD, and Dannis Chang, PharmD, of Halozyme are presenting the session “Leverage Technology and Innovative Tools to Enhance Publication and Medical Communication Deliverables” at Q1’s 8th Annual Medical Communications & Dissemination of Scientific Information Conference.

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Hitting Submission Timelines

Hitting Submission Timelines

by Allison McIlvain | Apr 23, 2019 | Life Science, Speaker Interview

Craig Gassman of Vericel Corporation is one of many experts featured at Q1 Productions’ 8th Annual Regulatory Operations & Submissions Conference in Philadelphia this June.

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11th Annual Life Science Strategic Patient Advocacy Engagement Conference

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3rd Annual Life Science Advertising & Promotion Conference

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12th Annual Medical Device and Diagnostic Labeling Conference

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Semi-Annual Medical Device Clinical Training & Education Conference

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Attendee Story: Senior Global RA Compliance Specialist, Hologic

Attendee Story: Senior Global RA Compliance Specialist, Hologic

by Allison McIlvain | Nov 26, 2019 | Attendee Story

Rene attended the 2nd Annual Life Science Regulatory Intelligence, Strategy & Execution Conference.

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Attendee Story: President/CEO/Founder

Attendee Story: President/CEO/Founder

by Allison McIlvain | Nov 25, 2019 | Attendee Story

Monica attended the 8th Annual Life Science Strengthening Patient Advocacy Engagement Conference.

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Attendee Story: Senior Director Clinical Science, Head of Medical Information, Alimera Sciences

Attendee Story: Senior Director Clinical Science, Head of Medical Information, Alimera Sciences

by Allison McIlvain | Nov 25, 2019 | Attendee Story

Erica attended the 6th Annual Customer Centric Medical Information Conference.

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Attendee Story: Business Development Manager, National Institute for Health Research

Attendee Story: Business Development Manager, National Institute for Health Research

by Allison McIlvain | Nov 25, 2019 | Attendee Story

Sarah attended the EU Medical Device Post-Market Clinical Evaluation Planning Conference.

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