There is a real opportunity for pharma to support the under-served population of atopic dermatitis patients, writes Mariel Metcalfe.
The need to look beyond the function’s traditional performance measures to the one that really matters-patient outcomes.
The need to look beyond the function’s traditional performance measures to the one that really matters-patient outcomes.
The need to look beyond the function’s traditional performance measures to the one that really matters-patient outcomes.
Impact, challenges and the importance of ensuring readiness with ICH E2B (R3) EudraVigilance.
Graham Francis sets out 5 critical business drivers for building a global enterprise labelling strategy over the year ahead.
A look into the complex battle between pharmaceutical manufacturers and payers for balance between medication access and budget management.
Kellie Rademacher identifies some of the key questions to consider when choosing an AI partner.
Meeting the stringent cloud compliance and regulatory requirements in pharma.
While digital transformation in life sciences starts with digitization for compliance, it should be seen as a key lever of competitive advantage and success, writes Jaleel Shujath.
How “patient influencers” look beyond price to help the industry evaluate newly-launched brands.
With digitalization enabling patient engagement with their own health experience more than ever before, two critical elements will steer pharma’s advertising path.
A discussion of the cost and time put into clinical trials.
A discussion of the cost and time put into clinical trials.
A discussion of the cost and time put into clinical trials.
KOLs have traditionally exerted their influence through research and publication on drug safety and efficacy, but now share the stage with other important measures.
Ashley Slavic details how Veeva Systems prepared for the EU data protection regulation, and what others can learn from the experience
A variety of consultant options are available to the pharma industry; this article is a 3-step guide to selecting the right consultant.
A variety of consultant options are available to the pharma industry; this article is a 3-step guide to selecting the right consultant.
Ellen Coleman outlines the highlights of a recent webinar on ensuring that patient advocacy is a key element of a market access strategy.
Global pharma companies and Japan can create a win-win situation through a new pricing mechanism, writes Nobuko Kobayashi.
As submissions complexity intensifies, the key to better resource management is better measurement, writes Adrian Leibert.
***Live: Tuesday, October 26, 2021 at 11 EDT | 8am PDT | 5pm CEST | 4pm BST*** Oracle Health Sciences reveals new research conducted to understand the technology adaptations that were made to clinical trials during the pandemic, the effect of these adaptations, and the impact of these changes on the future of clinical trials.
With so much information readily available companies have lost a significant level of control over how and when details about their progress in drug development and planning related to approval, launch, and commercialization are disseminated.
With so much information readily available companies have lost a significant level of control over how and when details about their progress in drug development and planning related to approval, launch, and commercialization are disseminated.
A discussion of the benefits that a cloud-based strategy has to offer.