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Articles
21.04.2016
Pharma preparing for NICE and EMA submissions

Pharma companies must start preparing its NICE submission at the time of making the regulatory subm...

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Articles
11.04.2016
Best practices for parallel scientific advice

A best practice guide for companies seeking parallel scientific HTA advice has been published by the...

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Articles
29.03.2016
Are HTA assessments here to stay

Whether ICER will become an integral part of the US healthcare landscape in the future remains to be...

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Articles
15.03.2016
International reference price methodologies

This report highlights some "quick wins" that member states can quickly and easily adopt to decrease...

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Articles
01.03.2016
Will the CDF proposals force pharma to prepare for...

From July 2016 NICE will gain decision power by saying yes, no or maybe to cancer drugs entering the...

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Articles
15.01.2016
Cost effective HTA evaluations

The methodology to be used within the cost-effectiveness HTA evaluations is likely to be based on a ...

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Articles
22.12.2015
Multi-country drug procurement

Some governments have looked to collective procurement with other countries, to in theory result in ...

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Articles
05.12.2015
Early payer scientific advice in the EU

There are now European platforms for seeking early scientific advice with multiple payer organisatio...

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Articles
25.11.2015
Securing earlier patient access

The aim of MAPPs is to enable quicker access for patients whilst providing adequate and evolving evi...

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Articles
20.11.2015
Are the PCSK9 Inhibitors the new Sovaldi

Based on the current clinical data, the PCSK9 inhibitors are a vital new treatment option for patien...

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