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Axiom edition 7
Spring 2013

Creating the functional pharma organisation

Value Communications v2.0

SafetyGauge

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Axiom edition 6
Autumn 2011

Engaging e-patients: How to steer pharma to safety

Value-based pricing in the UK: Developing an evaluation framework for burden of illness

Improving performance for pharmacovigilance inspections

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Axiom edition 5
Spring 2011

Focus on real-world data, including EU and US stakeholder research

In mint condition, the economic benefits of maintaining a
healthy workforce

China: access all areas? Reimbursement opportunities in China

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Axiom edition 4
Spring 2010

Focus on Talent management

Implementing patient access schemes in the UK

How can risk minimisation tools be improved?
An industry perspective

Innovation in patient compliance

Opinion on value demonstration

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Axiom Digest
2009

A collection of the best articles from Pope Woodhead's bi-annual newsletter

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Axiom edition 3
Spring 2009

The who, what, when and how of
local EU payer engagement

Registries: Real-world knowledge for competitive advantage

Has clinical trial disclosure helped the average patient?
An industry perspective

Focus on commercial innovation and risk sharing

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Axiom edition 2
Spring/Summer 2008

5 steps to an integrated value
proposition

PW’s ‘digital conversation’ risk
minimisation tool

Success factors for managing
key opinion leaders

Industry and payer perspectives
on cost-effectiveness evaluation

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Axiom edition 1
Autumn 2007

Opinion on Risk Management

Discussion of the five phases to
develop a successful mature
product portfolio

Perspective on the markets in
Poland and Spain

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Articles

China - Access all areas?

Rebecca Zhang
Wenting Zhang
Chris Easley

Pharmaceutical Market Europe
October 2012

Patient-Reported Outcomes (PROs) in safety adverse event reporting – a new framework

Anjan K Banerjee, DM, MBA, Simon Ingate, PhD,
Stephen Mayall, PhD,
Sally Okun, RN,
David Clifford,
Paul Wicks, PhD
and James Heywood.

Abstract poster from
DIA 2013

Behavioural assessment offers improved evaluation of risk minimisation tools (RMTs)

Anjan K Banerjee, DM, MBA, Simon Ingate, PhD, MBA,
Jon Mann,
Steve Hutson, PhD
and Rebecca Zhang, MD, PhD.

Abstract poster from
ICPE 2012

China: mapping the territory

Understanding the structure of China's healthcare reimbursement system is the first step to clearing the mist and visualising opportunities and challenges.

Pharmaceutical Market Europe July/August 2012

Risk Evaluation and Mitigation Strategies (REMS)

Detecting risk pre-market, managing risk post-approval, and the role of US and EU regulators

SCRIP Insights August 2011

Toolkit for patients’ organisations

Collaborative initiative to support groups in developing effective relationships with
key stakeholders

Pharmaceutical Market Europe September 2011

Lifestyle advice and drug therapy post-myocardial infarction: a survey of UK current practice.

Biosimilars: how to manage risks

PharmacoVigilance Review
Volume 3 Number 4
November 2009

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China: Access All Areas?

Wenting Zhang and
Chris Easley

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PW Guide to Services (Chinese)

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Communicating product
value to local payers is
a new challenge

Pharmaceutical
Marketing Europe
March/April 2009

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Innovative schemes give reassurance to payers in exchange for market access

Pharmaceutical
Marketing Europe
May/June 2009

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Risk rationale

Pharma needs a culture of
proactive pharmacovigilance
and risk minimisation

Pharmaceutical
Marketing Europe
July/August 2007

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Real Time Post Marketing Evaluation
of Therapeutic Risk Management
Plans(RMPs)

– A Novel Pharmacoepidemiological Tool?

Pharmacoepidemiology and Drug Safety 2008

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Better awareness and
implementation of
pharmacovigilance and
risk management planning
is needed within the European Pharmaceutical Industry

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Partnering patients

In this article Dr Beverly Barr discusses the long-term benefits of pharma engaging with patient organisations.

   

 

 

 


 

 

 


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