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Welcome

Pope Woodhead is a consulting group focused on the healthcare market. We deliver informed advice and pragmatic solutions to help our clients in the following areas:

Risk management
Drug safety
Regulatory affairs
Clinical development
Value communications
Market access
Product and portfolio management
External affairs
Talent and capability development
Business process innovation
Business productivity improvement

 


DIA 2013 49th Annual Meeting
Advancing Therapeutic Innovation and Regulatory Science
23-27 June 2013, Boston, US
Swapu Banerjee, Deputy Managing Director & Head of Regulatory, Risk & Clinical Development at Pope Woodhead will be delivering a tutorial on the topic:

Module VIII GVP

For more information about the event visit: DIA Annual Meeting


ISPOR 16th Annual European Congress
2-6 November 2013, The Convention Centre Dublin
Members from our Commercial practice will be participating and exhibiting at ISPOR’s 16th Annual European Congress in Dublin where we look forward to seeing you.

For more info about the event visit: ISPOR


BIT’s 1st Annual International Symposium of Clinical Trials & Hospital Management-2013
13-16 November 2013, Hainan International Convention and Exhibition Center, Haikou, China
Swapu Banerjee, Head of Regulatory, Risk & Clinical Development at Pope Woodhead will be chairing the session: Pharmacovigilance and Risk Management Strategies as well as delivering a presentation on evaluating the effectiveness of risk minimisation plans.

For more info about the event visit: Clinical Trials & Hospital Management-2013

 

8th Annual Pharma HR Forum Pharma Talent Forward 2013
Click here to read more and view the presentaion.


Spring 2013 edition of Axiom
now available, click here to view.


Seven rules for successful talent development programmes
click here to receive our
white paper.


Test your readiness for the new PV legislation
The new pharmacovigilance legislation that will come into force from the 2nd July 2012 will bring about substantial change in most Regulatory/ Pharmacovigilance departments.
To help you assess if your organisation is ready for them, PW have developed two questionnaires.
Click here to view.

 


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Informatics Value communications External affairs Business productivity improvement Business process innovation Talent and capability development Risk management Drug safety Regulatory affairs Clinical development Product and portfolio management Market access