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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News
06.10.2017
UK pharma denied legal challenge to drugs bill cap

The Association of British Pharmaceutical Industry has been refused a legal challenge to a cap on th...

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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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News
26.04.2017
PMA Perspective Q1 2017

Included in this issue is the implications for the UK market regarding Brexit and how the UKs CDF pe...

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Articles
05.03.2017
Managed entry agreements

MEAs are also known by other names such as risk-sharing agreements, value-added services, and result...

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