More Access and Evidence Articles

Access and Evidence

Quest for Available Drug Data Continues

Zuzanna Fimińska, (Feb 5, 2013)

The on-going battle for clinical trial data continues with calls from the European Parliament for drug makers to make full results widely available.
Access and Evidence

US Consumers Have Rosy View of Drug Costs

Louise Kelly, (Feb 5, 2013)

A new study from the W. P. Carey School of Business at Arizona State University shows consumers believe prices for essential medicines are based on public need and not profit.
Access and Evidence

Public Education: The Solution for Real World Evidence Privacy Concerns

Anonymous, (Jan 31, 2013)

Rochelle Sampy speaks to Richard Bergström, Director General of the European Federation of Pharmaceutical Industries and Associations about the benefits Real World Evidence can bring to healthcare and how to alleviate very valid concerns about data privacy.
Access and Evidence

The Patent War: MNCs Change Their Battle Strategy in India

Louise Kelly, (Jan 24, 2013)

With the Indian government continuing to favor generics in their quest for affordable healthcare, pharma multinationals are now opting for aggressive preemptive strikes to protect profits via India's courts.
Access and Evidence

Experts Call on FDA for Changes To “Unsafe” Medical Device Approvals

Anonymous, (Jan 24, 2013)

An academic perspective published in the New England Journal of Medicine makes an urgent call to the FDA to prevent unsafe medical devices from entering the marketplace.
Access and Evidence

China Proposes Fast-Tracking Registration for “High-priority” Generics

Ben Steele, (Jan 23, 2013)

China’s State Food and Drug Administration has announced proposals to reform the country’s drug registration process, including a special “fast-track” for generics which answer an unmet clinical need.
Access and Evidence

More Targeted, Personalised Treatments Expected from Pharma R&D Pipeline

Anonymous, (Jan 23, 2013)

Pharmaceutical companies are moving away from developing ‘blockbuster’ drugs to creating new targeted biopharmaceutical treatments for ‘niche’ diseases, according to recent research.
Access and Evidence

FDA Standards no Longer a Pain for NuPathe

Louise Kelly, (Jan 23, 2013)

The US Food and Drug Administration (FDA) has – for the first time – approved a patch that delivers the active drug transdermally to relieve migraine-related symptoms.
Access and Evidence

Health Committee Calling for a New Code of Practice

Zuzanna Fimińska, (Jan 22, 2013)

The Health Committee at the UK’s National Institute for Health and Clinical Excellence has urged the industry to rebuild trust with professionals and the public by making all clinical trial data available.
Access and Evidence

Merck’s Whistle Blowing Just Got Louder

Matthew Wood, (Jan 21, 2013)

After a storm of commotion in light of Merck & Co’s drug Tredaptive, which was found (when added to statins) not to reduce major vascular events as it’s supposed to, the company has taken it upon themselves to update the public on the latest developments.

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