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Pharmacovigilance, Drug Safety & Risk Management
11 May - 12 May 2015
Pharmacovigilance, Drug Safety & Risk Management

The expansive field of drug surveillance has increased the complexity of problems across the board in relation to PV auditing and meeting the standard requirements. Companies continue to face challenges of understanding the key considerations when presenting to auditors and knowing how to adequately adapt to different regulatory environments and changes. Moreover, clarifying individual roles within the PV system is paramount to setting out clear goals and meeting regulatory expectations.

For any company looking to globalise their business, the governance of reporting adverse drug events by different centralised authorities, along with heterogeneous terminologies and competing priorities has created greater uncertainties and barriers to enter new markets. The daunting task of complying with multiple regulations also heightens the danger of unrealistic expectations as well as mounting costs and time that will have long-term implications on investment.
Therefore, the importance of a centralised database has never been more vital to employ knowledge sharing and product awareness.

Join SAE Media Group in tackling these issues: 2015 will bring a focus on drug surveillance and signal detection; analysis and prevention of adverse drug reactions with MedDRA, industry experiences and global regulatory coverage of developments. Furthermore, we will cover Eudravigilance, and the growing trend of outsourcing Pharmacovigilance, as well as navigate through the challenges of compiling PSUR’s and frequent safety reports and how to adapt better to regulatory updates by preparing key areas that will be most impacted.
 

FEATURED SPEAKERS

Doris Stenver

Doris Stenver

Chief Medical Officer, Member of PRAC, Danish Health and Medicines Authority
Graeme Ladds

Graeme Ladds

CEO, Director of Operations, Pharmacovigilance, PharSafer Associates Ltd
Margot Stam Moraga

Margot Stam Moraga

Associate Director, Benefit-Risk Management , Quintiles
Peter De Veene

Peter De Veene

Executive Director, Clinical Safety and Pharmacovigilance (CSPV), Daiichi Sankyo
Pipasha Biswas

Pipasha Biswas

Executive Director & QPPV, Symogen Ltd
Tomas Moraleda

Tomas Moraleda

International Medical Officer, MedDRA MSSO

Alistair Coates

Director, EudraVigilance Consultants Ltd
Alistair Coates

Brian Edwards

Principal Consultant, NDA Regulatory Science Ltd
Brian Edwards

Chetan Shatapathy

Director, Sanjeevani Pharma
Chetan Shatapathy

Doris Stenver

Chief Medical Officer, Member of PRAC, Danish Health and Medicines Authority
Doris Stenver


Doris Irene Stenver, MD, MPA
Chief Medical Officer, Danish Health and Medicines Authority

Education
1986 Medical Degree from Copenhagen University, the Faculty of Medicine
2007 Master Degree in Public Administration, Copenhagen Business School

Clinical Experience
During 12 years (1986-1998) she worked at university hospitals in the Copenhagen area. In 1995 she became specialist in internal medicine. Her clinical experience covers nephrology, endocrinology, haematology, cardiology and infectious diseases. Her research activities were primarily within the areas of haematology, immunology, nephrology and endocrinology.

Regulatory Experience
She joined the Danish regulatory authorities and the EU Pharmacovigilance Working Party in 1998. In 2012 she became member of the Pharmacovigilance Risk Assessment Committee (PRAC). Her regulatory experience comprises all aspects of pharmacovigilance, including scientific evaluation of drug safety issues, development of risk management strategies, policies and guidelines, provision of scientific advice to the pharmaceutical industry, and communication to health care professionals and the public.
 

Graeme Ladds

CEO, Director of Operations, Pharmacovigilance, PharSafer Associates Ltd
Graeme Ladds

Julia Appelskog

QPPV , Bluefish Pharmaceuticals
Julia Appelskog

Short Bio

Dr. Julia Appelskog is the QPPV at Bluefish Pharmaceuticals. She is a member of the European Generic Association (EGA) and the Chairman of the Drug Safety and PV working Group at Swedish Generic Medicines Association (FGL).

She has more than 12 years of experience in Pharmacovigilance and 8 years of experience in biomedical research including experience in numerous therapy areas and product types such as medicinal products, including biopharmaceuticals and vaccines, medical device and cosmetics.

Julia hold different leading positions within pharmacovigilance in large pharma companies, such as MSD, Johnson & Johnson and Sanofi Pasteur MSD. Her expertise spans the entire product life cycle. She has been involved in variety of intervention and non-interventional epidemiological and clinical trials and was responsible for the Quality Assurance, Regulatory Affairs and Medical Information.

Dr. Appelskog has accomplished a PhD Thesis in cell biology at the Karolinska Institute (Sweden) in 2001, focusing on diabetes research. She has been a postdoctoral fellow at the Department of Clinical Neuroscience at Karolinska Institute, conducting research on epigenetic mechanisms, modification of DNA and its associated proteins in tumor cells. Julia is author of several scientific publications in diabetes and cancer research.

Julia was involved in the evaluation of diabetic drugs at Current Drugs LTD and was a member of working group creating case definitions in Brighton Collaboration, providing support to vaccine safety research. She has been a member of PV Focus Group at AESGP to shape the regulatory environment and have been an active member of PV Committee at the Pharmaceutical Industry in Sweden (LIF) for more than 7 years. Since 2006, she has been given several presentations within pharmacovigilance field.
 

Kashif Sheikh

Senior Safety Surveillance Advisor , Novonordisk
Kashif Sheikh

Lesley Wise

VP Global PV Risk Management & Pharmaepidemiology, Takeda
Lesley Wise

Bio


Dr. Lesley Wise is Vice President of Global PV Risk Management and Pharmacoepidemiology at Takeda, where she has responsibility for global risk management processes, benefit-risk assessment processes and implementation of risk management plans. In her current role, Lesley works closely with Pharmacovigilance, Regulatory and Medical Affairs colleagues to ensure a “joined up” approach to Benefit - Risk Management.

Lesley has a background in epidemiology and statistics, which is useful in implementing benefit risk methods. She is also an honorary lecturer at the London School of Hygiene and Tropical Medicine and an associate editor of Therapeutic Advances in Drug Safety.
 

Margot Stam Moraga

Associate Director, Benefit-Risk Management , Quintiles
Margot Stam Moraga

Bio

Margot has over 15 years of experience in the pharmaceutical industry. She has in-depth knowlegde in post-marketing pharmacovigilance and risk management, with a hands-on expertise in setting-up and implementation of safety signal management processes and signal detection methodologies.
Margot holds a Masters degree in Biochemistry, complemented with a Masters in Public Health and a Masters in Human Nutrition.
Prior to joining Quintiles, Margot was employed by Merck Serono for 14 years, where she held various positions with increasing responsibiility. In the Safety department she acted for 10 years as a safety product lead managing all pharmacovigilance aspects of several investigational and marketed products.
 

Mircea Ciuca

Head Medical & Clinical Drug Safety , Vifor Pharma
Mircea  Ciuca


Short Biography

 

Mircea Ciuca, MD, is Head of Medical & Clinical Drug Safety at Vifor Pharma Switzerland, where he is leading a team of scientists and physicians involved in all aspects of pharmacovigilance. Prior to joining Vifor Pharma he held various positions in Drug Safety at large pharmaceutical companies (MSD, Astellas) in The Netherlands, after he had successfully established and led the medical-scientific department of a medium-sized CRO in Rotterdam. Mircea is specialized in Emergency Medicine and Obstetrics & Gynecology, has been involved in clinical practice and academic teaching for about 12 years, and has about 10 years experience in drug safety.
 

Peter De Veene

Executive Director, Clinical Safety and Pharmacovigilance (CSPV), Daiichi Sankyo
Peter De Veene

Pipasha Biswas

Executive Director & QPPV, Symogen Ltd
Pipasha Biswas

Raquel Rogers

Medical Director Pharmacovigilance , Takeda UK Ltd
Raquel Rogers

Saad Shakir

Director, Drug Safety Research Unit
Saad Shakir

TBA

Principal Research Fellow , Drug Safety Research Unit
TBA

Tomas Moraleda

International Medical Officer, MedDRA MSSO
Tomas Moraleda

Conference agenda

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8:30

Registration & Coffee

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9:00

MedDRA Background & Coding Conventions

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9:30

Structure of MedDRA: Scope & Characteristics

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10:30

Morning Coffee

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11:00

MedDRA term selection: 'Points to Consider' documentation

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11:30

Hands-on practical exercises

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12:30

Close of Workshop

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13:30

Registration & Coffee

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14:00

Opening - From Safety Review to Signal Detection

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15:00

From Signals to Benefit-Risk assessments

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15:30

Coffee Break

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16:00

From Benefit-Risk to Risk minimisation

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17:00

Risk monitoring and modifications

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17:30

Close of Workshop

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8:30

Registration & Coffee

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9:00

Chair's opening remarks

Graeme Ladds

Graeme Ladds, CEO, Director of Operations, Pharmacovigilance, PharSafer Associates Ltd

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9:10

OPENING ADDRESS: Reaching the required performance standards of Pharmacovigilance

Graeme Ladds

Graeme Ladds, CEO, Director of Operations, Pharmacovigilance, PharSafer Associates Ltd

 

  • Evolve and diversify internal measures to best configure with diverse international regulation and updates  
  • Identifying market forces and events that influence Pharmacovigilance 
  • Clarifying the PV responsibilities of the innovator and generic company in partnerships
  • Recognizing where emerging trends, danger and money exist
  • Staying ahead of regulatory guidelines from multiple territories and technological innovation
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    9:50

    Reviews and infrastructure of Risk: Benefit management plans

    Lesley Wise, VP Global PV Risk Management & Pharmaepidemiology, Takeda

     

  • Identifying the issue and characterising the urgency of each risk to sustain balance
  • Managing the weight of evidence to aid risk analysis and decision making 
  • Adopting proactive approaches to communicating adverse events
  • Mitigating uncertainties and dangerous “unknowns” through systematic and structured quantitative methods 
  • A plan of action for risk minimization and benefit optimization
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    10:30

    Morning Coffee

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    11:00

    Combining adverse events throughout clinical trials and post-marketing surveillance

    Peter De Veene

    Peter De Veene, Executive Director, Clinical Safety and Pharmacovigilance (CSPV), Daiichi Sankyo

     

  • Emerging challenges to monitoring adverse drug events in clinical trials
  • Establishing key performance indicators for making timely safety reports and continuous quality improvements
  • Targeted event collection  
  • Solidifying communication patient- physician communication
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    11:40

    SPOTLIGHT PRESENTATION: Forecasting risk through signal detection analysis

    Margot Stam Moraga, Associate Director, Benefit-Risk Management , Quintiles

     

  • Optimising the predictive quality and information sought from signal detection
  • Validation and confirmation of risk and benefits from signal received  
  • Disproportionality screening analysis as a tool for signal detection and determining rare adverse events
  • Reducing the impact of the “masking” phenomenon
  • Emerging drug safety signals for report quality and content
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    12:20

    Networking Lunch

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    13:20

    MedDRA: Meeting evolving Pharmacovigilance needs

    Tomas Moraleda

    Tomas Moraleda, International Medical Officer, MedDRA MSSO

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    14:00

    Pharmacovigilance 2015 – greater integration and internationalization

    Doris Stenver, Chief Medical Officer, Member of PRAC, Danish Health and Medicines Authority

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    14:40

    Afternoon Tea

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    15:10

    Pharmacovigilance management & risk minimisation procedures to ensure drug safety

    Kashif Sheikh

    Kashif Sheikh, Senior Safety Surveillance Advisor , Novonordisk

     

  • Strengthening the link between a drug and its related adverse events from pre-clinical to post-marketing
  • Drug Safety & Product Life Cycle Management
  • Reporting of Signals & Risks
  • How to Measure the Effectiveness of Risk Minimisation Activities
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    15:50

    Combining adverse event monitoring and drug surveillance

    Chetan Shatapathy

    Chetan Shatapathy, Director, Sanjeevani Pharma

  • Core and emerging challenges to monitoring adverse drug events
  • Formulating improvements and establishing key performance indicators for continual quality assessment 
  •  Timely and effective benefit-risk communication to patients and physicians
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    16:30

    Panel Discussion: Advocating communication to enhance risk management and intellectual property

     

    • What are the core and emerging challenges of adhering to Pharmacovigilance laws and risk management?
    • How do we advocate towards a greater patient -centric system? 
    • What has been the main methodology developments used to monitor ADR's more rigorously? 
    • Does the shift towards emerging markets pose a risk to drug safety and biased data reports? 
    • How can communication between regulators, regional authorities and patients be further enhanced? 

    Graeme Ladds

    Graeme Ladds, CEO, Director of Operations, Pharmacovigilance, PharSafer Associates Ltd

    Tomas Moraleda

    Tomas Moraleda, International Medical Officer, MedDRA MSSO

    Margot Stam Moraga, Associate Director, Benefit-Risk Management , Quintiles

    Kashif Sheikh

    Kashif Sheikh, Senior Safety Surveillance Advisor , Novonordisk

    Chetan Shatapathy

    Chetan Shatapathy, Director, Sanjeevani Pharma

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    17:10

    Chair's Closing Remarks

    Graeme Ladds

    Graeme Ladds, CEO, Director of Operations, Pharmacovigilance, PharSafer Associates Ltd

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    8:30

    Registration & Coffee

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    9:00

    Chair's Opening Remarks

    Pipasha Biswas

    Pipasha Biswas, Executive Director & QPPV, Symogen Ltd

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    9:10

    Cause and Effect – Striving towards proactive surveillance through innovation

    Pipasha Biswas

    Pipasha Biswas, Executive Director & QPPV, Symogen Ltd

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    9:50

    Causality assessment of adverse drug events

    Brian Edwards

    Brian Edwards, Principal Consultant, NDA Regulatory Science Ltd

     

  • Performing up to standards: Requirements of the WHO-UMC causality assessment system
  • The strategy of pattern recognition and when it breaks down
  • Weighing the most useful information for decision making
  • Harness the impact of confounding factors
  • Determining the cause of rare adverse events
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    10:30

    Morning Coffee

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    11:00

    European drug safety under EudraVigilance

    Alistair Coates

    Alistair Coates, Director, EudraVigilance Consultants Ltd

    ·         Understanding the EudraVigilance System and where it fits within the entire European framework

    ·         How is it implemented in the pre- and post- marketing approval of medicinal drugs?

    ·         Challenges

    ·         Future outlook

     

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    11:40

    CASE STUDY: Good Pharmacovigilance (GPV) guidelines

    Julia Appelskog, QPPV , Bluefish Pharmaceuticals

     

  • Utilisation of PSUR’s as an effective Pharmacovigilance tool
  • Robust quality systems to ensure adequate and effective quality measures
  • Expectations and challenged of the PV system 
  • Organisational restructuring to adaptation to new updates
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    12:20

    Networking Lunch

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    13:20

    Post-marketing drug surveillance

    Saad Shakir

    Saad Shakir, Director, Drug Safety Research Unit

  • Best practice in design and conduct of PASS
  • Assessing risk: benefit using data from observational research
  • Barriers to quantifying adverse event/reactions
  • Informing on updates to drug labelling in post marketing
  • clock

    14:00

    Patient safety and tackling the challenges of under-reporting and patient communication

    Raquel Rogers

    Raquel Rogers, Medical Director Pharmacovigilance , Takeda UK Ltd

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    14:40

    Afternoon Tea

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    15:10

    CASE STUDY 2: Risk management for well-established products assessment

    Mircea Ciuca, Head Medical & Clinical Drug Safety , Vifor Pharma

  •  Benefit-risk profile for old products
  • Practicalities in building first RMP for well-established products
  • Monitoring risks – are routine PV activities enough?
  • clock

    16:30

    Chair’s Closing Remarks and Close of Day Two

    Pipasha Biswas

    Pipasha Biswas, Executive Director & QPPV, Symogen Ltd


    CEO, Director of Operations, Pharmacovigilance
    PharSafer Associates Ltd
    Executive Director & QPPV
    Symogen Ltd
    Director
    EudraVigilance Consultants Ltd
    QPPV
    Bluefish Pharmaceuticals
    Head Medical & Clinical Drug Safety
    Vifor Pharma
    VP Global PV Risk Management & Pharmaepidemiology
    Takeda
    Executive Director, Clinical Safety and Pharmacovigilance (CSPV)
    Daiichi Sankyo
    Associate Director, Benefit-Risk Management
    Quintiles
    International Medical Officer
    MedDRA MSSO
    Chief Medical Officer, Member of PRAC
    Danish Health and Medicines Authority
    Senior Safety Surveillance Advisor
    Novonordisk
    Principal Research Fellow
    Drug Safety Research Unit
    Director
    Sanjeevani Pharma
    Principal Consultant
    NDA Regulatory Science Ltd
    Medical Director Pharmacovigilance
    Takeda UK Ltd
    Director
    Drug Safety Research Unit

    Official Media Partner

    Supporters

    Workshops

    MedDRA Coding Guidelines

    MedDRA Coding Guidelines

    Holiday Inn Regents Park
    13 May 2015
    London, United Kingdom

    Risk Minimisation and Signal Management

    Risk Minimisation and Signal Management

    Holiday Inn Regents Park
    13 May 2015
    London, United Kingdom

    Attendee list for Pharmacovigilance 2015: Is your name on the list?

    Download

    Pharmacovigilance guidance on new legislation

    Download

    Media Partners


    The International Journal of Risk & Safety in Medicine

    Official Media Partner
    http://www.iospress.nl/journal/the-international-journal-of-risk-safety-in-medicine/

    The International Journal of Risk and Safety in Medicine is concerned with rendering the practice of medicine as safe as it can be; that involves promoting the highest possible quality of care, but also examining how those risks which are inevitable can be contained and managed. This is not exclusively a drugs journal. Recently it was decided to include in the subtitle of the journal three items to better indicate the scope of the journal, i.e. patient safety, pharmacovigilance and liability and the Editorial Board was adjusted accordingly.


    Pharmacovigilance Review

    Official Media Partner
    http://www.euromedcommunications.com/

    PharmacoVigilance Review: Journal on drug safety issues Editor – Rob Begnett This quarterly journal provides informed comment and analysis of international pharmaceutical regulations relating to the safe use of medicines and medicinal devices. It also carries reviews of current methods of pharmacovigilance. Order online at www.euromedcommunications.com Or email: publisher@euromedcommunications.com Tel: +44 (0)1428 752222 Fax: +44 (0)1428 752223

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    Drug Development Technology

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    http://www.drugdevelopment-technology.com

    Drugdevelopment-technology.com covers every aspect of the drug development and research process, from conception to pre-FDA approval. Our global network of journalists updates the site with the latest and most significant industry developments. This coverage allows us to provide everyone - from senior management through to research and QA staff – with in-depth reviews of the latest projects, advance notice of new product releases and analysis of the latest procedural and legislative developments.


    International Pharmaceutical Industry

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    http://www.ipimediaworld.com

    IPI gives you an insight into all areas of Biopharm, Medical, Pharmaceutical and Healthcare. IPI provides a proven supportive means of communication to the Pharmaceutical, Bio Pharmaceutical, Nutraceutical and Medical Devices industry, incorporating the latest in research and technology innovations, regulatory guidelines, marketing and communication strategies.


    Pharmaceutical Technology

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    http://www.pharmaceutical-technology.com

    Pharmaceutical-technology.com is the only website focusing specifically on issues relevant to pharmaceutical professionals working with technology, be it development, engineering, IT or production. Pharmaceutical-technology.com brings you the latest in industry projects and updates, along with the news, views and trends that leading professionals – from senior executives to manufacturing managers and heads of procurement – require to stay on top of their field.


    Labhoo

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    http://www.labhoo.com



    EIN News

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    http://www.einnews.com

    EIN News is the world leader in industry focused online news monitoring. Thousands of leading companies, institutions and global professionals from business, industry, and government rely on EIN News as an indispensable resource. Our systems continuously scan the web, indexing news from thousands of worldwide sources. The news you need is then organized by advanced software systems managed by a team of professional news editors. Everything we do is focused on streamlining your news searches and research in order to save you time and money.


    Bioportfolio Limited

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    http://www.bioportfolio.com

    BioPortfolio.com is a leading news, information and knowledge resource covering the global life science industries impacted by biotechnology. The site aims to provide the lay person, the researcher and the management executive with a single location to source core information on specific bio-related topics, to collate relevant data associated with each topic and to point the user to relevant knowledge resources


    Contract Biotechnology

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    http://www.contract-biotechnology.com

    Contract-Biotechnology.com is a web-based platform for laboratory outsourcing solutions. It is an online R&D matching tool that connects Scientifics and service and product providers worldwide. The platform Contract-Biotechnology.com would help you in the process of finding the right partner saving time and money, because with one single and secure application you would be able to receive multiple quotes quickly, keeping your contact information confidential. Contract-Biotechnology.com is the new Collaboration Network Model for Discovery Research and Development. Contract-Biotechnology.com team has extensive experience working for pharmaceuticals, biotechs, universities and academic research institutes and can help you addressing your key gaps.


    GenomeWeb

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    http://www.genomeweb.com

    GenomeWeb LLC is an independent, privately-held online and print publisher based in New York. Since 1997, GenomeWeb has served the global community of scientists, technology professionals, and executives who use and develop the latest advanced tools in molecular biology research and molecular diagnostics.

    GenomeWeb’s editorial mission is to serve readers with exclusive, in-depth coverage of the technology, institutions, and scientists that make up the worldwide research enterprise of molecular biology. We operate the largest online news organization focused on advanced research tools in genomics, proteomics, and bioinformatics.

    GenomeWeb readers can be found in major biopharmaceutical companies, top research universities, biomedical institutes, and government laboratories.


    Biosave

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    http://www.Biosave.com

    Biosave.com brings together the best Life Science promotions, product releases, featured products, publications, videos and events from 100’s of leading Life Science suppliers. Updated 24 hours a day, Biosave is constantly uploading special promotions and exciting product news that you won’t find anywhere else. Our goal is to provide our users with the most exclusive product information to help reach that all important purchasing decision.


    SelectScience

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    http://www.selectscience.net/register?utm_source=Media-Partner&utm_medium=Website&utm_campaign=SMI

    SelectScience is an independent, online information resource for the worldwide scientific community, and the home of trusted information for laboratory scientists. Discover the latest drug discovery and development technologies, products and techniques with product reviews, videos, application notes and news articles. Become a member for free today.


    Absave

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    http://www.absave.com

    Absave.com is the leading savings website for Antibodies and Immunological Products. Search our extensive database of Antibodies, Kits, Proteins & Peptides, Reagents, etc. to find the best savings!


    IOS Press

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    http://www.iospress.nl

    IOS Press publishes about 120 new books and 100 international journals each year covering topics ranging from computer science and mathematics to medicine and the natural sciences. All titles in this catalogue are available online as well as in print. Many titles are covered in the most important abstracting databases, such as Thomson Reuters / ISI, MEDLINE and SciVerse Scopus. Headquartered in Amsterdam with satellite offices in the USA, Germany, India and China, IOS Press has established several strategic co-publishing initiatives. Notable acquisitions included Delft University Press in 2005 and Millpress Science Publishers in 2008. IOS Press journals are available through the highly-regarded MetaPress platform.


    Pharmalicensing

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    http://www.pharmalicensing.com

    Pharmalicensing (www.pharmalicensing.com) is the premier biopharmaceutical Open Innovation resource designed for professionals involved with partnering, licensing and business development worldwide. Actively supporting all forms of partnering and in- and out-licensing activities, Pharmalicensing utilizes the unique online Showcase Profiling & Discover services, as well as its renowned Partnering Search service leveraging its global network of industry experts, to enable companies to identify and engage with appropriate partners around the world. Pharmalicensing is actively utilized by many tens of thousands of industry professionals each month. Pharmalicensing is a division of Cognis Group, Inc.


    Bioscreening

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    http://www.bioscreening.com



    Farmavita

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    https://farmavitar.com

    FarmavitaR+ is the professional network of experts and service providers. Network is gathering local consultants from 90 countries in Europe, Asia, North America, Latin America, Australia and Africa. Management of international, multi-centre projects is our core competence. FarmavitaR+ is providing solutions related to pharmaceutical, medical device, food supplement and cosmetic products. Scope of services is related to solutions for product development, quality assurance, clinical trials, product registration, portfolio analysis, lifecycle management, vigilance/risk management, pricing/reimbursing, market access and promotional compliance. FarmavitaR+ is brand name of Farmavita Regulanet Ltd. Visit https://farmavitar.com for more information. Outsource anything you can think of!

    Holiday Inn Regents Park

    Carburton Street
    London W1W 5EE
    United Kingdom

    Holiday Inn Regents Park

    Choose the well-connected Holiday Inn London-Regent's Park hotel, with a superb central London location and speedy transport links. Holiday Inn London-Regent's Park is in a leafy and cosmopolitan area of central London, a 10-minute walk from bustling Oxford Street. Leave your car in our NCP managed underground car park, and explore London by Tube. Great Portland Street Tube station is 25 metres from the hotel, from where you can reach the City and Canary Wharf in 30 minutes, and London Heathrow Airport in 45 minutes.

    Wireless Internet is available throughout the hotel, and you can invite up to 300 people to events at the Academy Conference Centre, with an IT technician and break-out zones. Holiday Inn London-Regent's Park is a 10-minute walk from Santander's offices and businesses in the BT Tower. Stroll 5 minutes to Regent's Park, where you'll find London Zoo and pretty Primrose Hill. We're a 10-minute walk from Bond Street boutiques and 20 minutes from Buckingham Palace and cruises on the River Thames.

    Ask our Concierge to plan your day out and book West End theatre tickets. Room Service is available 24 hours at Holiday Inn London-Regent's Park, or dine in the vibrant Junction Restaurant. Our Junction Bar has a menu of light bites, and a hot breakfast buffet is served daily.

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    WHAT IS CPD?

    CPD stands for Continuing Professional Development’. It is essentially a philosophy, which maintains that in order to be effective, learning should be organised and structured. The most common definition is:

    ‘A commitment to structured skills and knowledge enhancement for Personal or Professional competence’

    CPD is a common requirement of individual membership with professional bodies and Institutes. Increasingly, employers also expect their staff to undertake regular CPD activities.

    Undertaken over a period of time, CPD ensures that educational qualifications do not become obsolete, and allows for best practice and professional standards to be upheld.

    CPD can be undertaken through a variety of learning activities including instructor led training courses, seminars and conferences, e:learning modules or structured reading.

    CPD AND PROFESSIONAL INSTITUTES

    There are approximately 470 institutes in the UK across all industry sectors, with a collective membership of circa 4 million professionals, and they all expect their members to undertake CPD.

    For some institutes undertaking CPD is mandatory e.g. accountancy and law, and linked to a licence to practice, for others it’s obligatory. By ensuring that their members undertake CPD, the professional bodies seek to ensure that professional standards, legislative awareness and ethical practices are maintained.

    CPD Schemes often run over the period of a year and the institutes generally provide online tools for their members to record and reflect on their CPD activities.

    TYPICAL CPD SCHEMES AND RECORDING OF CPD (CPD points and hours)

    Professional bodies and Institutes CPD schemes are either structured as ‘Input’ or ‘Output’ based.

    ‘Input’ based schemes list a precise number of CPD hours that individuals must achieve within a given time period. These schemes can also use different ‘currencies’ such as points, merits, units or credits, where an individual must accumulate the number required. These currencies are usually based on time i.e. 1 CPD point = 1 hour of learning.

    ‘Output’ based schemes are learner centred. They require individuals to set learning goals that align to professional competencies, or personal development objectives. These schemes also list different ways to achieve the learning goals e.g. training courses, seminars or e:learning, which enables an individual to complete their CPD through their preferred mode of learning.

    The majority of Input and Output based schemes actively encourage individuals to seek appropriate CPD activities independently.

    As a formal provider of CPD certified activities, SAE Media Group can provide an indication of the learning benefit gained and the typical completion. However, it is ultimately the responsibility of the delegate to evaluate their learning, and record it correctly in line with their professional body’s or employers requirements.

    GLOBAL CPD

    Increasingly, international and emerging markets are ‘professionalising’ their workforces and looking to the UK to benchmark educational standards. The undertaking of CPD is now increasingly expected of any individual employed within today’s global marketplace.

    CPD Certificates

    We can provide a certificate for all our accredited events. To request a CPD certificate for a conference , workshop, master classes you have attended please email events@saemediagroup.com

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    Contact SAE Media Group

    UK Office
    Opening Hours: 9.00 - 17.30 (local time)
    SAE Media Group , Ground Floor, India House, 45 Curlew Street, London, SE1 2ND, United Kingdom
    Tel: +44 (0) 20 7827 6000 Fax: +44 (0) 20 7827 6001
    Website: http://www.smgconferences.com Email: events@saemediagroup.com
    Registered in England - SMi Group Ltd trading as SAE Media Group




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