Articles
04.11.2020
Has NICE increased speed of patient access

... and the use of financial arrangements for new oncology and non-oncology drugs?

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Articles
28.10.2020
EMA regulatory decisions after BREXIT

The UK will continue to adopt decisions taken by the European Commission on the approval of new mark...

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Articles
26.10.2020
What is critical appraisal of evidence

When critically appraising a clinical study, it is key to firstly identify the sources of uncertaint...

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Articles
23.10.2020
Sustainable biosimilar marketplaces

To facilitate biosimilar uptake, several mechanisms encouraging biosimilar uptake have been implemen...

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Articles
12.10.2020
What impact has COVID-19 had on HTA bodies

A survey of employees within pricing and market access n pharma and biotech companies.

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Articles
22.09.2020
Update and validate legal price certificates

Remap Consulting are ideally placed to support the completion of price certificates ready for legali...

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Articles
17.09.2020
The value of a Global Value Dossier

GVD is a core document, which may be considered the “heart” of the pharmaceutical product’s pa...

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Articles
09.09.2020
Early access to medicines in the UK

This newsletter will discuss the early access processes operating within the UK and discuss the adva...

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Articles
13.08.2020
What is Health Technology Assessment (HTA)

A multidisciplinary process that uses explicit methods to determine the value of a health technology...

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Articles
29.07.2020
Real world data included in NICE

How has the data available within NCRAS been utilized within the CDF overseen by NICE, in partnershi...

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