Clinical Research Market in Poland. Barbara Kozierkiewicz



Similar documents
History and Principles of Good Clinical Practice

Oversight of Clinical Trials in Europe - Member State perspective. Gunnar Danielsson Senior Expert Pharmaceutical Inspector

White Paper CLINICAL RESEARCH IN POLAND AN INTRODUCTION

Clinical Trial Logistics

Data Management and Good Clinical Practice Patrick Murphy, Research Informatics, Family Health International

Moving from Compliance to Competency for the Clinical Research Professional

Adjudication in Oncology Trials: A Concept Whose Time Has Come

Conducting Clinical Trials in Turkey

The Clinical Trials Directive in the EU: Present and Future Elisabethann Wright, Partner Maurits Lugard, Partner. May 2010

Advancing research: a physician s guide to clinical trials

BioWorld s PARTNER in FOCUS: Covance AN ADVERTISING SERVICE FROM BIOWORLD

and Regulatory Aspects

INVITATION LETTER ASSIGNMENT TITLE: INDIVIDUAL CONSULTANCY SERVICES RELATED TO THE TRAINING ON ADVANCED GCP TRAINING FOR RBC/MRC.

The Concept of Quality in Clinical Research. Dorota Śwituła Senior Clinical Quality Assurance Advisor

What is necessary to provide good clinical data for a clinical trial?

Professional Standards and Guidelines

Serious Breaches. Ian Gravenor. Senior Clinical Project Manager Novo Nordisk Ltd

Salary Survey Domestic, International Salary Survey and Country Cost Analysis

de formation continue Diploma of Advanced Studies Management of Clinical Trials Good Clinical Practice Implementation and Quality Processes

Laboratory medicine as one of the pharmacists competencies

Even we will get to use your product someday. Enough reason for us to deliver.

Social health insurance in Belgium. Charlotte Wilgos & Thomas Rousseau

Reflection paper on the Use of Interactive Response Technologies (Interactive Voice/Web Response Systems) in Clinical Trials

White Paper CLINICAL RESEARCH IN BELGIUM AN INTRODUCTION

TABLE OF CONTENTS International Transfer Pricing in the Ethical Pharmaceutical Industry Second edition

Sheffield Kidney Institute. Planning a Clinical Trial

School of Pharmacy TEMPLE UNIVERSITY

Future Specialisation for Pharmacists in Industry

Extemporaneously Prepared Early Phase Clinical Trial Materials

WORKSHOP. Health Economics

EMA Update Clinical Trials

Emergence of Compassionate Use programmes

New Scientist/SRG Salary Survey 2013

Essential Documents for Clinical Trial Research. Centre for Health Evaluation and Outcome Sciences Manager, Clinical Research Development Office

Global Policy on Interactions with Healthcare Professionals

Türkiye İlaç ve Tıbbi Cihaz Kurumu

The Role of Regional Medical Advisor (RMA)-Field Medical. Dr. Aju Abraham Varghese Pfizer India. Feb 22 nd 2014

EU Clinical Trials Register. An agency of the European Union

Quality Management in Clinical Trials

Health Care Job Information Sheet #20. Clinical Research

CERTIFICATE IN CLINICAL TRIAL MANAGEMENT

Position Statement on Doctors' Relationships with Industry 2010

Practical Image Management for

CLINICAL TRIALS WITH MEDICINES IN EUROPE

A PROVEN APPROACH to ACCELERATED CLINICAL DEVELOPMENT

The Clinical Trials Process an educated patient s guide

THE BIOTECH & PHARMACEUTICAL INDUSTRY

GLP vs GMP vs GCP Dominique Pifat, Ph.D., MBA The Biologics Consulting Group

Clinical Trial Trends Outline Complexity for Supply Chain. Scott Ohanesian, VP Commercial Operations APAC

Medical Writing in Focus A Med Comms Agency Perspective. Mike Thompson Scientific Director, Complete Medical Group

Health Insurance. Perception & Reality. Salman Rawaf MD PhD FRCP FFPH. Professor of Public Health Erbil Iraq 2-4 Feb 2011 s.rawaf@imperial.ac.

Automating Cell Biology Annual general meeting, September 7, Phase Holographic Imaging

Patient Search in Clinical Trials history, current trends and technological advances

Roles & Responsibilities of the Sponsor

Paediatric Rheumatology InterNational Trials Organization PRINTO

Course Certificate In. Pharmaceuticals and Medical Research: Clinical Research Monitoring & Coordination

The Role of Actuaries in Poland

Department of Chemistry and Biochemistry Academic Career Advising and Mentoring

Expected Growth of Industry-Sponsored Clinical Trials in the Middle East Benchmarked on other Global Regions

BioMed Partners. The rocky way from science to market. Dr. Karsten Fischer BioMedPartners AG. VPM Days Hannover

The Japan Society of Mechanical Engineers C 2010

EU DIRECTIVE ON GOOD CLINICAL PRACTICE IN CLINICAL TRIALS DH & MHRA BRIEFING NOTE

Safety Risk Management Company Perspective

Diabetes Trends in the U.S.: Results from the National Health and Wellness Survey. White Paper. by Kathy Annunziata and Nikoletta Sternbach

Medicines for Human Use (Clinical Trials Regulations) 2004

Pharmaceutical Quality & Clinical Research Quality: The Interaction

Manchester Pharmacy School.

Data Quality in Clinical Trials: a Sponsor's view

Novartis Methodological Note

Clinical trials submitted in marketing-authorisation applications to the European Medicines Agency

The European regulatory system for medicines and the European Medicines Agency

European Forum for Good Clinical Practice Audit Working Party

Location for Trials- Global Considerations A Pharma Perspective. Carlo Maccarrone Assoc. Director, Clinical Research GSK Australia 7 May 2014

Presented at: Jefferies 2015 Global Healthcare Conference

Workshop on Quality Risk Management Making Trials Fit for Purpose

Hollie Goddard Sr. IRB Coordinator McKesson Specialty Health

Managing Risk in Clinical Research. Dr Martha J Wrigley R&D Manager Senior Visiting Fellow University of Surrey

Regulated Applications in the Cloud

Quality by Design Concept

Amgen GLOBAL CORPORATE COMPLIANCE POLICY

2009 Foley & Lardner LLP Attorney Advertising Prior results do not guarantee a similar outcome Models used are not clients but may be representative

How companies leverage quality and quality certifications to achieve competitive advantage

STANDARD OPERATING PROCEDURE FOR RESEARCH. 2. Notification of Serious Breaches of Good Clinical Practice or Study Protocol

ITALY POLAND JOINT SCIENCE AND TECHNOLOGY COOPERATION CALL FOR JOINT PROJECT PROPOSALS CLOSING DATE: 10/06/2015

Transcription:

Clinical Research Market in Poland Barbara Kozierkiewicz

Agenda Why pharma R&D? Clinical trials introduction Clinical trials market in Poland Opportunities and challenges Global vs. local clinical research market value Clinical trial market employees

Business R&D investments Pharmaceuticals and biotechnology sector amounts to 18,1% of total business R&D expenditure worldwide. According to the 2013 EU Industrial R&D Investment Scorecard Source: The Pharmaceutical Industry in Figures, Key Data, 2014, European Federation of Pharmaceutical Industries and Associations

Pharma Industry R&D investment in Europe Source: The Pharmaceutical Industry in Figures, Key Data, 2014, European Federation of Pharmaceutical Industries and Associations

Clinical trial trials to evaluate the effectiveness and safety of medications or medical devices by monitoring their effects on agroups of people. Preclinical Phase I Phase II Phase III PhaseIV (postregistration) may be conducted by government health agencies, researchers affiliated with a hospital or university medical program, independent researchers, or pharma industry.

Clinical trial sponsors

History Clinical research on a large scale developed at the beginning of the last century in the US, Canada, Japan and Western Europe. Global GCP standards introduced in the industry in 1996 initiated globalization trends in this area. Industry started to search for new markets. At the same time political and economic changes meant that Poland became the reliable market for this activity. Joining the EU and adoption of EU Directives governing the conduct of clinical trials facilitated this activity even more.

Clinical trials in Poland Source: 1. Data for 2003-2009 Badania kliniczne w Polce Główne wyzwania, PWC, listopd 2010 2. Data for 20010-14 Office for registration of medical products, medical devices and biocidal products. Average phase distribution I 10%, II 30%, III 55%, IV 5%)

Source: Clinical Trial Magnifier, Feb 2009 Investigator sites location

Trends

Challenges Sensitive business Lack of knowledge in society or negative public perception 1, 2 60% 50% 40% 30% 20% 10% 0% My work is widely known in the community Disagree Neither agree nor Agree agree Audit performed in Poland in 2009 by National Chamber of Control in 13 Teaching Hospitals showed deficiencies in the financial aspect of this business3 The quality of the research done in this part of Europe was questioned by some scientists from established markets4 Sources: 1. GCPpl Assotianions reports, June 2014 2. Own research, a sample of 52 polish employees of pharma research companies and CRO 3. National Chamber of Control, Audit report, December 2010 2. Glickman et al., Ethical and scientific implications of the globalization of clinical research. New England Journal of Medicine, 2009.

Employment in R&D in Europe Source: The Pharmaceutical Industry in Figures, Key Data, 2014, European Federation of Pharmaceutical Industries and Associations

Clinical trails market employees in PL In 2010 it was estimated that 1200 Clinical Research Associates work in Poland1 Physicians, pharmacists and other medicine related professions, many on PhD degree Do not regret changing profession Satisfied with the new profession (important, interesting, self-realization)2 Sources: 1. Badania kliniczne w Polsce Główne wyzwania, PWC, listopad 2010 2. Own research, a sample of 52 polish employees of pharma research companies and CRO

Clinical research market employees I regret that I do not do the profession consistent with my education. 50% 40% 30% 20% 10% 0% Disagree Neither agree nor Agree agree I would be happy to take a very big effor to return to the learned profession: physician, pharmacist, biologist, biotechnologist,... 40% 30% 20% 10% 0% Disagree Neither agree nor Agree agree Source: Own research, a sample of 52 polish employees of pharma research companies and CRO

Clinical research market employees 60% 50% 40% 30% 20% 10% 0% agree My job is important Agree Neither agree nor Disagree 60% 50% 40% 30% 20% 10% 0% agree My work is challenging and demanding Agree Neither agree nor Disagree 60% My job is interesting I have a high degree of autonomy at work 50% 40% 30% 20% 10% 0% agree Agree Neither agree nor Disagree 45% 40% 35% 30% 25% 20% 15% 10% 5% 0% agree Agree Neither agree nor Disagree Source: Own research, a sample of 52 polish employees of pharma research companies and CRO

Further development in Poland The marketis still developing and, what is more important new, higher level R&D activities, like central data management or global R&D organizations are being established Source: Warsaw Business Journal,1012,Investment of the Year Award