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Articles
05.01.2017
How NICE is coping with managing the CDF

This process aims to be completely transparent , to enable faster patient access to oncology treatme...

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News
19.12.2016
PMA Perspective Q4 2016

Topics covered include are payers helping or hindering biosimilar market access as well as can MCDA ...

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Articles
05.12.2016
Theory of multiple criteria decision analysis

Multi-criteria decision analysis (MCDA) is a potentially useful tool that can be used to support dec...

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Articles
21.11.2016
Potential changes to NICE

NICE has recently published a consultation on changes to its appraisal process to "fast track" some ...

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Articles
05.10.2016
Challenges for biosimilar market access

Biosimilars have the potential to be considered comparable to generics and offer healthcare benefits...

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Articles
22.09.2016
NICE to charge for appraisals

NICE propose to charge to conduct single technology appraisals from May 2017.

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Articles
15.06.2016
The challenge in securing patient access

Enabling physicians to identify patients who are most likely to respond to treatment thereby achievi...

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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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News
30.03.2016
PMA Perspectives Newsletter- March 2016

Topics include our perspectives on an EU commission report on how international reference pricing ca...

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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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