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Articles
05.02.2018
A single, mandatory HTA assessment for Europe

Over the last year, the European Commission (EC) has been consulting on multiple scenarios for HTA h...

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Articles
28.01.2018
The arrival of gene therapies

The development of gene therapies represents a new frontier of science, with the potential to help p...

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Articles
17.11.2017
Market Access Training

Remap Consulting are proud to announce that we are hosting two, 1 day market access training worksho...

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Articles
13.11.2017
NICE's Modified Cancer Drugs Fund Process

This study investigates NICE evaluations of new cancer indications and legacy CDF indications (not p...

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Articles
23.10.2017
Pricing and reimbursements for biosimilars

Paul Craddy is proud to be presenting at the Global Pharmaceutical Regulatory Affairs Summit in Prag...

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Articles
20.09.2017
Market Access Training

Our training courses are designed to help your organization to understand market access and what it ...

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Articles
05.08.2017
Pricing and market access skills

Obtaining market access at the right time and at an appropriate price has become more complex for ph...

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Articles
05.07.2017
No confidential discounts in Germany

Introduction of a new German Act - Strengthening Pharmaceutical Supply in the Statutory Health Insur...

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Articles
05.06.2017
EMA has published Q&A document

EMA has published Q&A document to prepare manufacturers for the UK's withdrawal from the EU with reg...

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Articles
05.06.2017
New parallel consultation process

A one stop shop for joint advice between EMA, EUnetHTA and health technology assessment bodies - the...

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