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Superbugs & Superdrugs USA
November 12 - November 13, 2018
Superbugs & Superdrugs USA

SAE Media Group’s 3rd Annual Conference
Superbugs & Superdrugs USA 
November 12 - 13, 2018 | Iselin, New Jersey
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The issue of antibacterial resistance is becoming increasingly prevalent within the world of modern medicine. Difficult-to-treat pathogens create an incredibly real issue within clinical environments; and the problem needs to be addressed with novel treatments and the development of mechanisms which circumvent current therapeutic barriers.The push to commercialization of novel anti-infectives is also a big barrier to market entry within the field; with red-tape and funding restrictions creating hindrances to the progress of anti-infective drugs through trial and regulatory approvals processes.

To address the ever-growing need of informative and thought provoking discussion, in order to address these industry issues, Superbugs & Superdrugs USA conference will offer a jam-packed agenda with presentations from key industry leaders and up-and-coming thinkers, within the field.

Register to attend by September 28 to save $100 on booking fee
 

LETTER FROM CHAIRS
"While recently approved antibiotic agents will likely help stem AMR crisis, novel approaches to the prevention and treatment of MDR infections are needed to ensure a viable antimicrobial armamentarium for the future.
The SAE Media Group's Superbugs & Superdrugs USA meeting will bring together expertise from individuals in multiple disciplines in the field of infectious disease representing research, regulatory, funding, diagnostics and academia to focus on supporting antimicrobial research and development, funding opportunities and resources for companies, new diagnostics for clinical applications, as well as novel therapies and approaches"

William J. Weiss - UNT System College of Pharmacy
A. Simon Lynch - Janssen Research & Development



 

FEATURED SPEAKERS

Andrew Tomaras

Andrew Tomaras

VP and Director of Microbiology, BacterioScan Inc.
Antonio DiGiandomenico

Antonio DiGiandomenico

Principal Scientist, MedImmune
Brent Cezairliyan

Brent Cezairliyan

Senior Scientist, Octagon Therapeutics
Ian Friedland

Ian Friedland

Clinical Consultant, Ex-Chief Medical Officer, Achaogen
Mark Albrecht

Mark Albrecht

Project Officer, HHS/ASPR/BARDA

Andrew Tomaras

VP and Director of Microbiology, BacterioScan Inc.
Andrew Tomaras

Dr. Tomaras is currently Vice President and Director of Microbiology at BacterioScan, Inc, where his roles include new product/protocol development and the design and oversight of clinical regulatory activities. He received his BA and PhD degrees from the Department of Microbiology at Miami University in 2000 and 2004, respectively. His subsequent postdoctoral research was conducted at the University of Colorado Health Sciences Center. He joined the Antibacterials Research Unit at Pfizer in 2008, and helped to start the Endogenous Human Biologic Response group as a Senior Principal Scientist within the Biotherapeutics Division in 2011.

Anita Sheoran

Therapeutics Development Project Officer, NIAID, NIH
Anita Sheoran

Anita Sheoran is Program Officer at NIAID’s Drug Development Section in Division for Microbiology and Infectious Diseases where she provides technical and business oversight of a multimillion-dollar antibacterial drug development portfolio of NIAID funded contracts. She is NIAID’s liaison to CARB-X and serves as a member of its Scientific Review Boards. Also, she serves as steering committee member of Defense health funded wound infection prevention and management task area at Military Infectious Diseases Research Program. Prior to joining NIAID, she held several positions in public and private sector supporting pre-clinical to the early clinical phase development of drugs against multi-drug resistant bacteria and fungi

Anthony Simon Lynch

Senior Scientific Director, Janssen Fellow & Incubator Leader, Janssen
Anthony Simon Lynch

Antonio DiGiandomenico

Principal Scientist, MedImmune
Antonio DiGiandomenico

Dr. Antonio DiGiandomenico is currently a Principal Scientist in the Department of Microbial Sciences at MedImmune/AstraZeneca and has 20 years of experience in microbiology and immunology. Dr. DiGiandomenico began his training in molecular biology and microbial pathogenesis at Duquesne University and continued his doctoral training at the University of Virginia. Upon completion of a postdoctoral fellowship at Vanderbilt University, Dr. DiGiandomenico accepted a position at MedImmune in 2009. Since arriving at MedImmune, Dr. DiGiandomenico has focused on the development of novel immunotherapeutics against multi-drug resistant bacteria in multiple disease settings and has contributed to pre-clinical and clinical programs.

Brent Cezairliyan

Senior Scientist, Octagon Therapeutics
Brent Cezairliyan

Dr. Cezairliyan is Vice President of Microbiology at Octagon Therapeutics. He has studied bacterial pathogenesis as a geneticist and a biochemist for over 15 years. Prior to Octagon, Dr. Cezairliyan worked at Massachusetts General Hospital and Harvard Medical School where he studied the regulation of bacterial virulence under fellowships from the NIH and the Cystic Fibrosis Foundation. Dr. Cezairliyan received his Ph.D. from the Massachusetts Institute of Technology, where he studied signaling mechanisms in bacterial proteostasis.

Christopher Ford

Group Leader, Microbiome Sciences of ID, Seres Therapeutics
Christopher Ford

Daniel Pevear

Sr. Vice President of Biology and Grants Development, Venatorx Pharmaceuticals
Daniel Pevear

Dr. Pevear is the Senior Vice President of Biology and Grants Development at VenatoRx Pharmaceuticals Incorporated, which he co-founded in 2010 with Drs. Christopher Burns (CEO) and Luigi Xerri (CDO). Dr. Pevear has over 30 years of experience in both biotech and big pharma, with stints at Sterling Winthrop, ViroPharma (co-founder), Progenics, Novartis and Protez Pharmaceuticals. He received in Ph.D. in 1984 from Rensselaer Polytechnic Institute in Viral Immunology, and was a Multiple Sclerosis Post-Doctoral Fellow at Northwestern University Medical School with Dr. Howard Lipton. Dr. Pevear has over 60 peer-reviewed publications and has co-authored several book chapters.

Ian Friedland

Clinical Consultant, Ex-Chief Medical Officer, Achaogen
Ian Friedland

Dr. Friedland is currently a consultant, focusing on advising companies on early and late development of anti-infective products. He trained as a pediatric infectious disease specialist at UT Southwestern Medical Center in Dallas. He served as the chief medical officer at Achaogen from 2014 to 2017, where he was responsible for leading the clinical development, regulatory strategy and medical affairs functions. Prior to Achaogen, Dr. Friedland headed the clinical development of numerous antibiotics at Cubist pharmaceuticals. He has worked in the pharmaceutical and biotechnology industry for 20 years, at both large Pharma (Merck, J&J) and several small biotech companies, leading clinical development teams of several important antibiotics and has played a pivotal role in the submission in the US, EU and other regions of drugs including ertapenem, caspofungin, doripenem, alvimipan, fidaxomicin, ceftolozane/tazobactam and plazomicin, in addition to supporting many marketed anti-infective agents. He is a frequent participant in a number of FDA/FNIH/PhRMA infectious disease working groups. He is an author on over 100 peer reviewed journal articles and book chapters.

Joe Newman

Senior Director, Head of Biology, Tetraphase Pharmaceuticals
Joe Newman

Dr. Newman, has over 25 years of experience in the fields of microbiology, animal model development and pharmacology. Prior to joining Tetraphase, Dr. Newman worked at Triad Therapeutics and AstraZeneca. During this period, he was involved in four programs which are currently in clinical development. Dr. Newman was also responsible for new model development at AstraZeneca, including in vivo models of MDR/XDR Enterobacteriaceae spp. and A. baumannii. During his tenure at Tetraphase Dr. Newman has been responsible for writing the nonclinical section of the Eravacycline NDA and MAA submissions, and is the principal Investigator on the TP-6076 CARB-X grant.

Laura Kovanda

Senior Director Global Development Project Leader, Astellas Pharma Global Development, Inc.
Laura Kovanda

Mahmoud Ghannoum

Director of Center for Medical Mycology, Case Western Reserve University
Mahmoud Ghannoum

Dr Mahmoud Ghannoum received MSc in Medicinal Chemistry and PhD in Microbial Physiology from University of Technology in England, and an MBA from the Weatherhead School of Management at Case. Presently he is a tenured Professor and Director of the Center for Medical Mycology, Case Western Reserve University and University Hospitals Case Medical Center (UH) where he established a multidisciplinary disciplinary Center of Excellence that combines basic and translational research investigating microbes from the test tube to the bedside. He is also a fellow of the Infectious Disease Society of America and past President of the Medical Mycological Society of the Americas (MMSA). In 2016, Dr Ghannoum received the Rohda Benham Award presented for his continuous outstanding and meritorious contributions to medical mycology from the Medical Mycological Society of the Americas and he also received the Freedom to Discover Award from Bristol-Myers Squibb for his work on microbial biofilms.

Mark Albrecht

Project Officer, HHS/ASPR/BARDA
Mark Albrecht

Stephanie Noviello

V.P Clinical Development, MotifBio
Stephanie Noviello

Stephanie Noviello joined Motif Bio in May 2018 from Bristol-Myers Squibb, where she was the Virology Clinical Program Lead for the hepatitis B, hepatitis C and HIV portfolios. She previously worked at Schering-Plough Research Institute in Hepatology. Prior to working in industry, she was an Epidemic Intelligence Service Officer at the Centers for Disease Control and Prevention stationed with the New York State Department of Health Bureau of Communicable Disease Control. She is a board-certified pediatrician, and received her M.D. from Tulane University School of Medicine and her M.P.H. from the Tulane University School of Public Health and Tropical Medicine.

Stephen Barat

Head of Pre-Clinical and Early Clinical Development, SCYNEXIS Inc
Stephen Barat

Stephen A. Barat, PhD, is currently the Head of Preclinical Research and Early Development for Scynexis. Dr. Barat has more than 20 years of global drug development and registration experience across multiple therapeutic areas. Prior to joining Scynexis, he served in various leadership positions in preclinical development in Allergan, Forest Laboratories, and Schering-Plough. Dr. Barat is also a recognized expert in the interface between safety assessment and CMC requirements and is a member of the PQRI working group for leachables from parenteral drug products and the USP expert panel on biocompatability of packaging materials. He has spoken extensively in numerous international venues on a variety of topics on drug development.

William Weiss

Director of Pre-Clinical Services, University of North Texas Health Science Center
William Weiss

sponsors

Conference agenda

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8:30

Registration & Coffee

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9:00

Opening Remarks & Introductions

David Perlin

David Perlin, Executive Director & Professor, Public Health Research Institute, Rutgers University

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9:15

Session 1: What is the landscape for current molecular diagnostic development

  • What technology is available
  • What platforms have been developed and are approved
  • What is the promise and impact of the new technology
     
  • Tom Lowery

    Tom Lowery, Chief Scientific Officer, T2 Biosystems

    Brendan  Manning

    Brendan Manning, Associate Director Molecular Diagnostics, T2 Biosystems, Inc.

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    10:00

    Session 2: How is this technology viewed by regulatory authorities

    Ribhi M. Shawar

    Ribhi M. Shawar, Branch Chief, General Bacteriology and Antimicrobial Susceptibility Branch, Food and Drug Administration

  • How does FDA see the role of this technology
  • What are the special considerations that govern approval
  • What is the role of post-approval monitoring in this space
  • Are new rules needed?
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    10:30

    Morning Coffee

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    11:00

    Session 3: “A real-life clinical view of molecular diagnostic technology”

    David Perlin

    David Perlin, Executive Director & Professor, Public Health Research Institute, Rutgers University

  • What is the clinical value?
  • What obstacles remain to be overcome
  • Can it deliver on its promise?
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    11:40

    Q&A

    David Perlin

    David Perlin, Executive Director & Professor, Public Health Research Institute, Rutgers University

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    12:30

    Chairman’s Closing Remarks and Close of Day One

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    13:30

    Registration & Coffee

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    14:00

    Opening Remarks & Introductions

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    14:10

    Session 1: Environmental analysis

  • Current and future market dynamics:  US and Europe
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    14:50

    Session 2: Proposed solutions and incentives

  • Critical success factors for delivering a successful launch
  • Legislative/ policy proposals private/public partnerships, how do we fix the ‘broken’ market
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    15:20

    Afternoon Tea

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    15:50

    Session 3: The implementation of these solutions into the market place

  • Case study - A recent launch
  • Developing a commercial strategy for pipeline antibiotics
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    16:30

    Session 4: Q&A

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    17:00

    Closing Remarks and End of Workshop

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    8:30

    Registration & Coffee

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    9:00

    Chairman's Opening Remarks

    William Weiss

    William Weiss, Director of Pre-Clinical Services, University of North Texas Health Science Center

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    9:10

    Discovery and evaluation of inhibitors of intermediary metabolism as novel antibiotics against Gram-negative bacterial pathogens

    Brent Cezairliyan, Senior Scientist, Octagon Therapeutics

  • Identification of growth conditions that stimulate virulence of the human pathogen Pseudomonas aeruginosa
  • A screening platform to identify novel compounds that inhibit bacterial growth under virulence-stimulating conditions
  • Inhibitors of central metabolism exhibit in vivo activity against P. aeruginosa and Acinetobacter baumannii infections
     
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    9:50

    Pathogen-focused drug development: buyer beware

    Ian Friedland, Clinical Consultant, Ex-Chief Medical Officer, Achaogen

  • The development of new antimicrobial agents following current regulatory pathways remains challenging if the development is aimed at addressing resistant or single species gram negative pathogens
  • The recent passage of LPAD (limited population antimicrobial drug) pathway legislation raised the promise of greater flexibility in accepting smaller datasets for approval of drugs addressing an uncommon unmet need
  • However, what this means in practical terms is still unclear 
  • Recent experience with the development and approval of plazomicin for an unmet need indication has been disappointing and will be discussed 
     
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    10:30

    Morning Coffee

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    11:00

    VNRX-5133: a highly potent and broad-spectrum inhibitor of both serine and metallo beta-lactamases

    Daniel Pevear, Sr. Vice President of Biology and Grants Development, Venatorx Pharmaceuticals

  • VNRX-5133 is a boronic acid that exhibits direct, selective and potent inhibitory activity against bacterial serine and metallo-b lactamases
  • VNRX-5133 rescues cefepime activity in strains of ESBL- and carbapenemase-expressing Enterobacteriaceae and Pseudomonas aeruginosa
  • VNRX-5133 is a b-lactamase inhibitor that lacks stand-alone antibacterial activity
  • VNRX-5133 rescues cefepime activity in vivo in multiple animal models of bacterial infection
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    11:40

    TP-6076: A novel fluorocycline antibiotic with potent activity against carbapenem-resistant Gram (-) organisms

    Joe Newman, Senior Director, Head of Biology, Tetraphase Pharmaceuticals

  • TP-6076 is a potent inhibitor of bacterial protein synthesis
  • The activity of TP-6076 is not affected by the common mechanisms of Gram (-) resistance
  • TP-6076 demonstrates potent activity in murine thigh and lung infections
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    12:20

    Networking Lunch

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    13:20

    Iclaprim, an antibiotic differentiated from other antibiotics for serious and life-threatening infections

    Stephanie Noviello, V.P Clinical Development, MotifBio

  • Activity against nonsusceptible MRSA isolates to standard of care antibiotics
  • Concentration at sites of infection
  • Suppresses bacterial toxin production
  • Not nephrotoxic, no renal dosing or therapeutic drug monitoring required
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    14:00

    Immunotherapeutics targeting Pseudomonas aeruginosa acute and persistent infections

    Antonio DiGiandomenico, Principal Scientist, MedImmune

  • Introduce novel anti-Pseudomonal mAbs and their mechanisms of action
  • Activity will be discussed in multiple animal models when used in both prophylaxis and treatment indications
  • Activity against biofilms will also be presented
  • Synergy with antibiotic treatment will also be discussed
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    14:40

    Afternoon Tea

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    15:10

    The state of developments within the anti-fungal space

    Mahmoud Ghannoum, Director of Center for Medical Mycology, Case Western Reserve University

  • What is the status of resistance in terms of fungal pathogens?
  • What are the main fungal strains posing the greatest threat to public health?
  • Which are the current anti-fungals currently in use?
  • Where are the gaps in anti-fungal development, which need to be addressed?
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    15:50

    SCY-078: A first-in-class, orally-bioavailable, glucan synthase inhibitor has broad spectrum activity against Candida, Aspergillus and Pneumocystis spp

    Stephen Barat, Head of Pre-Clinical and Early Clinical Development, SCYNEXIS Inc

  • Effects of SCY-078 against multi-drug resistant fungal pathogens
  • Results from preclinical PK/PD models for Candida, Aspergillus and Pneumocystis spp
  • Discussion on pharmacokinetic characteristics of SCY-078, including disposition profile
  • Applications in the treatment of life-threatening infections
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    16:30

    Supporting antibacterial research and development

    Mark Albrecht

    Mark Albrecht, Project Officer, HHS/ASPR/BARDA

  • What is BARDA and why is it interested in AMR
  • How BARDA partners with industry to stimulate innovation in AMR R&D
  • How CARB-X is refilling the preclinical AMR product pipeline
     
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    17:10

    Chairman’s Closing Remarks and Close of Day One

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    8:30

    Registration & Coffee

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    9:00

    Chairman's Opening Remarks

    Anthony Simon Lynch

    Anthony Simon Lynch, Senior Scientific Director, Janssen Fellow & Incubator Leader, Janssen

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    9:10

    Update on epidemiology, resistance and treatments of GI related infectious disease

    William Weiss

    William Weiss, Director of Pre-Clinical Services, University of North Texas Health Science Center

  • Advances in the diagnosis and treatment of Clostridium difficile infections
  • Helicobacter pylori - Latest research and news
  • Drug-resistant intestinal bugs - Salmonella, Shigella, and Yersinia
  • Gut microbiome: a new player in gastrointestinal disease
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    9:50

    NIAID funding and resources for development of anti-infectives

    Anita Sheoran, Therapeutics Development Project Officer, NIAID, NIH

  • NIAID strategic plan for CARB and support for development of novel therapeutic classes
  • Overlapping funding strategies and a broad spectrum of preclinical and clinical services that educe product development risk
  • Current funding and partnership opportunities for development of antibacterials. 
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    10:30

    Morning Coffee

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    11:00

    The Microbiome and its impact on the field

    Christopher Ford

    Christopher Ford, Group Leader, Microbiome Sciences of ID, Seres Therapeutics

  • An overview of the current research being done into the microbiome, with applications to antimicrobial development
  • Anti-pathogenic properties of certain substances being produced by some microbes
  • A case study of clostridium difficile infections – an imbalance in the gut microbiome
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    11:40

    Practical clinical diagnostic applications using laser light-scattering: utility, adoption, and opportunities

    Andrew Tomaras, VP and Director of Microbiology, BacterioScan Inc.

  • Production of accurate and affordable platform for widespread clinical use
  • Performance of current clinical application for rapid urinary tract infection detection
  • Developmental applications including other direct-from-specimen infection detection and phenotypic antimicrobial susceptibility testing
  • Platform utilization to streamline new antimicrobial clinical trial enrolment and clinical adoption
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    12:20

    Networking Lunch

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    13:20

    Pharmacokinetic and Pharmacodynamic approaches to optimize drug development in invasive Aspergillosis

    Laura Kovanda

    Laura Kovanda, Senior Director Global Development Project Leader, Astellas Pharma Global Development, Inc.

    PK-PD techniques to better estimate dosage regimens
    Validation of preclinical models and controls to be used for future compounds in IA
    Possibility of using biomarker as endpoints in clinical trials of IA
     

     

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    14:40

    Chairman’s Closing Remarks and Close of Day Two

    Anthony Simon Lynch

    Anthony Simon Lynch, Senior Scientific Director, Janssen Fellow & Incubator Leader, Janssen

    clock

    14:50

    Post Conference Refreshments


    VP and Director of Microbiology
    BacterioScan Inc.
    Therapeutics Development Project Officer
    NIAID, NIH
    Senior Scientific Director, Janssen Fellow & Incubator Leader
    Janssen
    Principal Scientist
    MedImmune
    Senior Scientist
    Octagon Therapeutics
    Group Leader, Microbiome Sciences of ID
    Seres Therapeutics
    Sr. Vice President of Biology and Grants Development
    Venatorx Pharmaceuticals
    Clinical Consultant, Ex-Chief Medical Officer
    Achaogen
    Senior Director, Head of Biology
    Tetraphase Pharmaceuticals
    Senior Director Global Development Project Leader
    Astellas Pharma Global Development, Inc.
    Director of Center for Medical Mycology
    Case Western Reserve University
    Project Officer
    HHS/ASPR/BARDA
    V.P Clinical Development
    MotifBio
    Head of Pre-Clinical and Early Clinical Development
    SCYNEXIS Inc
    Director of Pre-Clinical Services
    University of North Texas Health Science Center

    Sponsors and Exhibitors

    Official Media Partner

    Official Associations

    Supporting Media Partners

    Infographic for Superbugs & Superdrugs USA

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    Interview with Dr. Brent Cezairliyan - Octagon Therapeutics

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    Interview - Stephanie Noviello, Motif Bio

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    Interview with Laura Kovanda, Astellas Pharma Global Development, Inc.

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    Presentation by Cara Cassino, ContraFect

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    Presentation by William J. Weiss, University of North Texas Health Science Center

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    Presentation by Richard Alm, Macrolide Pharmaceuticals

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    Presentation by Christopher McMaster, DeNovaMed

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    Presentation by Nicole Mahoney, Merck

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    Presentation by Mark Albrecht, BARDA

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    [Interview] - Daniel Pevear, Venatorx Pharmaceuticals

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    [Interview] - Mark Albrecht, HHS/ASPR/BARDA

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    [Programme] - Superbugs & Superdrugs USA

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    [Speaker Line-up]

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    [LETTER FROM CHAIRS]

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    [Attendee list]

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    [Workshop A] - Programme

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    [Workshop B] - Programme

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    Sponsors and Exhibitors


    SCYNEXIS

    Sponsors and Exhibitors
    http://www.scynexis.com

    SCYNEXIS, Inc. (NASDAQ: SCYX) is a biotechnology company committed to positively impacting the lives of patients suffering from difficult-to-treat and often life-threatening infections by delivering innovative anti-infective therapies. The SCYNEXIS team has extensive experience in the life sciences industry, discovering and developing more than 30 innovative medicines over a broad range of therapeutic areas. The Company's lead product candidate, SCY-078, is a novel IV/oral antifungal agent in Phase 2 clinical and preclinical development for the treatment of several serious and life-threatening invasive fungal infections caused by Candida and Aspergillus species. For more information, visit www.scynexis.com.

    Media Partners


    American Pharmaceutical Review

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

    Start receiving your free copy today. American Pharmaceutical Review is a review of the drug pipeline from the late discovery phase through manufacturing. American Pharmaceutical Review prides itself on having the most relevant, unbiased and informative editorial in the industry. You will find that all of our editorial is highly technical and written by government agencies, consultants, academics, and large pharmaceuticals companies. American Pharmaceutical Review covers several key topics that are important to drug production:Separations and purification, Drug Delivery, Biopharmaceutical Processing, Biopharmaceutical Development, Formulation development, Manufacturing, Microbiology, Instrumentation, Spectroscopy

    Media Partners


    Technology Networks

    Supporting Media Partners
    http://go.technologynetworks.com/subscribe-to-newsletters

    Founded in 2000, Technology Networks is established as the leading news provider for life science and drug discovery professionals. In addition, we provide unique content including webcasts, videos, application notes and posters from recent conferences. Our portfolio now includes around 30 focussed scientific communities, all of which are accessible free of charge within TechnologyNetworks.com


    pharmaphorum

    Supporting Media Partners
    http://www.pharmaphorum.com

    pharmaphorum drives innovation within the pharmaceutical industry, by bringing healthcare together through a suite of media services that help produce and disseminate thought leadership, combined with an online platform for communicating messages to a global audience.Visit www.pharmaphorum.com


    Gate2Biotech

    Supporting Media Partners
    http://www.gate2biotech.com

    Gate2Biotech is a portal that unites biotechnological community in Central Europe. It covers all the news in the field of biotechnology. Thanks to the the portal the companies engaged in the field can easily search for research institutions and other partners to solve technical problems they are facing and here they can also present their services offer to potential partners from the Czech Republic and abroad. Gate2Biotech portal serves as a bridge connecting scientific and commercial sector. It incorporates offices and support organizations dedicated to promoting transfer of innovative technologies into a unified communication platform of Czech and international biotechnologies. As a mediator of information it draws attention to biotechnologies and support of their application and transfer into practice. It also functions as a tool for encouraging non-professionals (especially scientists and students) towards innovative business or applied research.


    Pharmaceutical Outsourcing

    Supporting Media Partners
    http://www.pharmoutsourcing.com

    Pharmaceutical Outsourcing, the journal dedicated to pharmaceutical and biopharmaceutical contract services. With regular sections on contract manufacturing, contract research, contract packaging, formulation/development services, contract analytical testing, APIs, stability testing, clinical research and other areas, we bring the most complete coverage of trends and issues in the industry to our 15,000 readers in North America.


    Pharma Journalist

    Supporting Media Partners
    http://www.pharmajournalist.com

    Pharma Journalist is a product of Kellen Media. Pharma Journalist is one of the leading website covering the need of global Pharmaceutical Industry. Articles like latest news, trends, analysis, market report, press releases, whitepapers, case studies, etc. published on pharmajournalist.com helps Industry professionals and decision makers to stay on the top of this fast-paced industry. Pharma Journalist aims of providing fast and informative articles to its readers and subscribers.


    World Pharma News

    Supporting Media Partners
    http://www.worldpharmanews.com/



    Drug Discovery Today

    Supporting Media Partners
    http://www.drugdiscoverytoday.com/

    Drug Discovery Today covers the whole of the preclinical drug discovery process. The reviews are cutting edge, written by experts in their respective fields and cover all aspects of drug discovery from genomic and proteomic approaches, computational drug design, medicinal chemistry and the translation of these sciences to therapies.


    Global Biodefense

    Supporting Media Partners
    http://www.globalbiodefense.com/

    Global Biodefense publishes the latest news on vaccine and therapeutics countermeasure development, biosurveillance and detection technologies, food safety and biosecurity, and CBRN incident preparedness and response. Visit our website to access daily news updates, organization profiles, conference listings, and the latest in funding opportunities for advancing biodefense technology.


    Biocompare

    Supporting Media Partners
    http://www.biocompare.com

    Biocompare.com is the leading resource for up-to-date product information, product reviews, and new technologies for life scientists. Biocompare combines an in-depth knowledge of life science products and new technologies with the power of the Internet to offer scientists the most dynamic, relevant, and innovative media-based marketplace for life science information.


    American Laboratory

    Supporting Media Partners
    http://www.americanlaboratory.com

    For laboratory managers and researchers utilizing analytical chemistry and its applications, seeking knowledge on new technologies, methods, applications, and products, the American Laboratory® publication platform provides comprehensive technology coverage for laboratory professionals at all stages of their careers. Unlike single-channel publications, American Laboratory® is a multidisciplinary resource that engages scientists through print, digital, mobile, multimedia, and social channels to provide practical information and solutions for cutting-edge results. American Laboratory® serves the need of global community of laboratory professionals for communicating relevant technical advances and insights. Globally, American Laboratory® reaches out to subscribers by offering digital distribution plus premium print in North America. Digital communications utilize internet, mobile and social channels.


    Pharmalicensing

    Supporting Media Partners
    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


    Infectious Diseases Hub

    Supporting Media Partners
    http://www.id-hub.com

    Infectious Diseases Hub is a free-to-access website open to all researchers, students and anyone else who might have an interest in the many aspects of microbiology and virology. We offer easy access to breaking news, interviews, opinion pieces, peer-reviewed articles and multimedia features, with a strong focus on the rising issue of antimicrobial resistance. Microbiology is such a diverse and exciting area, and with the emergence of new technologies giving us the ability to study complex communities and rapidly sequence whole genomes, there has been something of a ‘revolution’. Keeping on top of such technological advances and the latest emerging diseases is at the heart of Infectious Diseases Hub, and you can take a look at up-to-date essential research and information on the site now.


    IPI

    Supporting Media Partners
    http://www.ipimediaworld.com

    IPI – International Pharmaceutical Industry Established by professionals with over 30 years experience in the Pharmaceutical and Life sciences publishing sectors. We have identified the needs of these dynamic industries, and have listened carefully to our readers and advertisers. With strong collaboration between Pharmaceutical and Life sciences Industry Associations we have created a global distribution network. We give you a promise to become a reliable extension of your marketing and communication arm. If necessary we will integrate our expertise with your needs. Incorporating new and innovative communication methods we will help to highlight your expertise.

    Official Associations


    Swiss Biotech Association

    Official Associations
    http://www.swissbiotech.org/

    The Swiss Biotech Association (SBA) is the national industry association for biotechnology, including pharmaceuticals, diagnostics, agriculture, food, cosmetics, environmental biotechnology, and specialty chemicals. Members are companies active in modern biotechnology, such as R&D, Production, Marketing and Sales, Finance, Services and Consulting. SBA provides a networking platform for Life Science clusters, academic and federal institutions the like. Founded in March 1998, the Association grows steadily.

    Renaissance Woodbridge Hotel

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    USA

    Renaissance Woodbridge Hotel

    Your simple delights will become memorable moments at Renaissance Woodbridge Hotel. This distinctive hotel in Edison, New Jersey, features 269 modern guest rooms, including 42 suites, and more than 25,000 square feet of flexible meeting space. Our hotel's location is centrally located amidst corporate offices and tourist attraction. Our accommodations stand out from other hotels in Edison, NJ, and provide a sophisticated retreat for families and business travelers alike. Marriott's Plug-in panels and 37-inch LCD HD TVs allow guests simultaneous connectivity to laptops, iPods and DVD players. We are one of the most conveniently situated hotels at the crossroads of U.S. Routes 1 and 9. We are also just five minutes from Woodbridge Center Mall, 15 minutes south of Newark Liberty International Airport (EWR) and less than one mile from the Metropark train station. With our premier location and amenities, our Edison accommodations provide an advantageous travel destination.

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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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