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Lyophilisation USA

 

There’s a growing demand for lyophilised pharmaceutical products that are contributing to an increase in the adoption of lyophilisation equipment and the need for lyophilised biopharmaceuticals and other formulations in the pharmaceutical industry. This is contributing to the projected rise in investment, currently dominated by North America, which is expected to reach $4.80 billion in 2020. This rate of growth is a result of new biologics and biosimilars, enhancing the need for lyophilisation equipment and services.
 

 

The requirements governed by the FDA and supported by ISPE focus on improving patient safety and product quality – supporting the adoption of lyophilisation in pharmaceutical manufacturing, with the necessity to lyophilise APIs and various formulations such as antibodies, antiviral drugs, insulin, biosimilars, injections and other therapeutic proteins.
 

FEATURED SPEAKERS

Akhilesh  Bhambhani

Akhilesh Bhambhani

Principal Scientist, Novel Adjuvants, Formulations and Delivery Technologies, Merck & Co. Inc.
Andrea  Weiland-Waibel

Andrea Weiland-Waibel

Managing Director, Explicat Pharma GmbH
Graham Magill

Graham Magill

Engineer I, Pharmaceutical Processing and Technology Development, Genentech, Inc.
James Searles

James Searles

Technical Fellow, Global Manufacturing Science and Technology, One 2 One Hospira
Lindsay Wegiel

Lindsay Wegiel

Research Associate III, Baxter Pharmaceutical Solutions, LLC
Paul Coiteux

Paul Coiteux

Director of Technical Sales, SP Scientific
Reingard Schandl

Reingard Schandl

Project Manager, Global Technology Transfer, Baxter BioScience
Ronald Pate

Ronald Pate

Lyophilization Development Scientist, Patheon Pharmaceuticals Inc.
Sune Andersen

Sune Andersen

Drying Processes and Particle Technology in CMC, Novo Nordisk A / S
Swapnil Pansare

Swapnil Pansare

Associate Scientist - I, Formulation Sciences, MedImmune Inc
T.N. Thompson

T.N. Thompson

President, Millrock Technology, Inc.
Tudor Arvinte

Tudor Arvinte

Professor University of Geneva, Chairman & CEO, Therapeomic Inc., University Of Geneva
Vikram Sadineni

Vikram Sadineni

Senior Research Investigator, BMS

Akhilesh Bhambhani

Principal Scientist, Novel Adjuvants, Formulations and Delivery Technologies, Merck & Co. Inc.
Akhilesh  Bhambhani

Andrea Weiland-Waibel

Managing Director, Explicat Pharma GmbH
Andrea  Weiland-Waibel

Barry D Moore

CSO, Xstalbio Ltd
Barry D Moore

Graham Magill

Engineer I, Pharmaceutical Processing and Technology Development, Genentech, Inc.
Graham Magill

James Searles

Technical Fellow, Global Manufacturing Science and Technology, One 2 One Hospira
James Searles

Jamie Tsung

Principal Scientist, Momenta Pharmaceuticals Inc
Jamie Tsung

Katherine Giacoletti

Senior Statistician, Arlenda
Katherine Giacoletti

Kevin Ward

Director of R&D , BioPharma Technology
Kevin Ward

Lindsay Wegiel

Research Associate III, Baxter Pharmaceutical Solutions, LLC
Lindsay Wegiel

Paul Coiteux

Director of Technical Sales, SP Scientific
Paul Coiteux

Reingard Schandl

Project Manager, Global Technology Transfer, Baxter BioScience
Reingard Schandl

Ronald Pate

Lyophilization Development Scientist, Patheon Pharmaceuticals Inc.
Ronald Pate

Sune Andersen

Drying Processes and Particle Technology in CMC, Novo Nordisk A / S
Sune Andersen

Swapnil Pansare

Associate Scientist - I, Formulation Sciences, MedImmune Inc
Swapnil Pansare

T.N. Thompson

President, Millrock Technology, Inc.
T.N. Thompson

Tim Paymaster

President, Ellab Inc
Tim Paymaster

Tudor Arvinte

Professor University of Geneva, Chairman & CEO, Therapeomic Inc., University Of Geneva
Tudor Arvinte

Vikram Sadineni

Senior Research Investigator, BMS
Vikram Sadineni

sponsors

Conference agenda

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8:30

Registration & Coffee

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9:00

Welcome and Opening Remarks

Kevin Ward

Kevin Ward, Director of R&D , BioPharma Technology

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9:10

Basic Principles of QbD and what it means for lyophilization

Kevin Ward

Kevin Ward, Director of R&D , BioPharma Technology

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9:30

Defining Critical Quality Attributes and a Target Product Profile for a lyophilized product

Kevin Ward

Kevin Ward, Director of R&D , BioPharma Technology

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10:00

Risk minimization and "Risk Dynamics" in Freeze-Drying

Kevin Ward

Kevin Ward, Director of R&D , BioPharma Technology

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10:30

Morning Coffee

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11:00

Building a Design Space:

Kevin Ward

Kevin Ward, Director of R&D , BioPharma Technology

  • The interplay between equipment, formulation and process
  • Integration of formulation and process design/development
  • Looking at the balance between desktop studies and lab trials
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    12:00

    Final interactive discussion session and summing up

    Kevin Ward

    Kevin Ward, Director of R&D , BioPharma Technology

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    12:30

    End of Workshop

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    8:30

    Registration & Coffee

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    9:00

    Chairs Opening Remarks

    Andrea  Weiland-Waibel

    Andrea Weiland-Waibel, Managing Director, Explicat Pharma GmbH

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    9:10

    Cycle development basic concepts and optimising the process

    Ronald Pate

    Ronald Pate, Lyophilization Development Scientist, Patheon Pharmaceuticals Inc.

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    9:50

    Transfer of Lyophilization Processes

    Reingard Schandl

    Reingard Schandl, Project Manager, Global Technology Transfer, Baxter BioScience

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    10:30

    Advances in Temperature Mapping inside Lyophilizers

    Tim Paymaster

    Tim Paymaster, President, Ellab Inc

  • Real-time wireless temperature data
  • Wireless Vacuum measurement
  • Accessories for Probe placement
  • Advanced Data Analysis Features
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    11:10

    Morning Coffee

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    11:40

    Improving Lyophilisation Process Efficiency via Primary Drying Optimisation

    Swapnil Pansare

    Swapnil Pansare, Associate Scientist - I, Formulation Sciences, MedImmune Inc

    clock

    12:20

    New Formulation Technologies for Stabilisation of Therapeutic Proteins and Vaccines

    Akhilesh  Bhambhani

    Akhilesh Bhambhani, Principal Scientist, Novel Adjuvants, Formulations and Delivery Technologies, Merck & Co. Inc.

  • Enabling Technologies for Formulation Development
  • Case Studies documenting enhanced stability of vaccines and Monoclonal(s) in newly enabled formulation
  • Summary and Path Forward
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    13:00

    Networking Lunch

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    14:00

    Case Study: Adapting a lyophilization cycle from pirani to capacitance manometer gauge pressure control

    James Searles

    James Searles, Technical Fellow, Global Manufacturing Science and Technology, One 2 One Hospira

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    14:40

    Leveraging Sophisticated Modelling in QbD - Why Bother?

    Katherine Giacoletti

    Katherine Giacoletti, Senior Statistician, Arlenda

  • What are the desirable elements of a modelling method?
  • Introduction to Bayesian Methods
  • Application of Bayesian Methods to QbD for lyophilisation
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    15:20

    KEYNOTE ADDRESS: Applying QbD to Freeze-Drying: Space and Time, Risks and Practicalities

    Kevin Ward

    Kevin Ward, Director of R&D , BioPharma Technology

  • The challenge of applying a QbD approach to a process with a dynamic risk profile
  • How can we visualise a Design Space for freeze-drying?
  • Balancing desktop studies with practical lyophilisation
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    16:00

    Afternoon Tea

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    16:30

    Drug Product Development Using a QbD approach for Commercialization

    Vikram Sadineni

    Vikram Sadineni, Senior Research Investigator, BMS

  • DoE Based Approach to Process Development
  • Application of Modeling Tools in Process Scale-up and Commercialization
  • clock

    17:10

    Primary Drying Optimization Using a Three-Dimensional Design Space

    Lindsay Wegiel

    Lindsay Wegiel, Research Associate III, Baxter Pharmaceutical Solutions, LLC

  • Objectives and need for a 3D based approach
  • Modeling of a 3D design space
  • Case studies with a mannitol sucrose system
  • clock

    17:50

    ROUND TABLE DISCUSSION

    Andrea  Weiland-Waibel

    Andrea Weiland-Waibel, Managing Director, Explicat Pharma GmbH

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    18:30

    Chairs Closing Remarks and Close of Day One

    Andrea  Weiland-Waibel

    Andrea Weiland-Waibel, Managing Director, Explicat Pharma GmbH

    clock

    8:30

    Registration & Coffee

    clock

    9:00

    Chairs Opening Remarks

    Andrea  Weiland-Waibel

    Andrea Weiland-Waibel, Managing Director, Explicat Pharma GmbH

    clock

    9:10

    KEYNOTE ADDRESS: Hot and cold spot determination to allow for process control by use of Product Temperature Tp PAT Device

    Andrea  Weiland-Waibel

    Andrea Weiland-Waibel, Managing Director, Explicat Pharma GmbH

  • Use of the Real Time PAT to control the freeze-drying cycle
  • Dynamic Hot and Cold Spot Determination as Performance Qualification
  • Evaluation/Definition of most critical "hot and cold spots" to be instrumented with the real time PAT Device
  • clock

    9:50

    Freeze Drying PAT using Heat Flux Measurement

  • Overview of Heat Flux Sensing, the latest Process Analytical Technology that works in both freezing and primary drying
  • Heat Flow during freezing effects ice crystal formation. Examine how different freezing profiles effect primary drying times. Examine how controlled nucleation may/may not have an impact on shortening primary drying
  • Measuring heat flow during primary drying enables protocol development for easy process transfer
  • T.N. Thompson

    T.N. Thompson, President, Millrock Technology, Inc.

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    10:30

    Morning Coffee

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    11:00

    Controlled Nucleation in Production Lyophilizers: Current State of Technology

    Paul Coiteux

    Paul Coiteux, Director of Technical Sales, SP Scientific

  • Controlled nucleation has shown in development labs to offer significant benefits, including shortened primary drying cycles.
  • ControLyo TM Nucleation On-Demand Technology has been both incorporated into new production dryers and retrofit onto existing dryers.
  • The results of two retrofit studies done with major Pharma companies will be presented
  • clock

    11:40

    Spray drying as an alternatvie to freeze drying

    Sune Andersen

    Sune Andersen, Drying Processes and Particle Technology in CMC, Novo Nordisk A / S

  • Aseptic drying for parenterals – spray vs. freeze drying
  • Nanoparticles by freeze drying and spray drying approaches
  • QbD – comparison between spray and freeze drying
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    12:20

    Networking Lunch

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    13:30

    INDUSTRY INSIGHT - An example solution

    Graham Magill

    Graham Magill, Engineer I, Pharmaceutical Processing and Technology Development, Genentech, Inc.

  • Discuss the application of Praxair ControLyo controlled ice nucleation technology to optimize the lyophilization of a low glass transition temperature (Tg’), high fill volume product
  • Assessing the impact of processing parameters such as ice nucleation temperature and post-nucleation cooling ramp rate on cake microstructure will be discussed
  • clock

    14:10

    Case Study: The role of physical chemistry in freeze-drying from product characteristics to process performance

    Tudor Arvinte

    Tudor Arvinte, Professor University of Geneva, Chairman & CEO, Therapeomic Inc., University Of Geneva

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    14:50

    Afternoon Tea

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    15:20

    Concentrated solid dosage formulations of therapeutic biologics

    Barry D Moore

    Barry D Moore, CSO, Xstalbio Ltd

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    16:00

    Concentrated dosage formulations effecting biologics and solid therapeutics

    Jamie Tsung

    Jamie Tsung, Principal Scientist, Momenta Pharmaceuticals Inc

  • A perspective on the scale of the challenge faced and the methods to be reviewed as a solution
  • Is reconstitution using centrifugation the answer?
  • Ensuring high dosage delivery of proteins
  • clock

    16:40

    Chairs Closing Remarks and Close of Day Two

    Andrea  Weiland-Waibel

    Andrea Weiland-Waibel, Managing Director, Explicat Pharma GmbH


    Principal Scientist, Novel Adjuvants, Formulations and Delivery Technologies
    Merck & Co. Inc.
    Lyophilization Development Scientist
    Patheon Pharmaceuticals Inc.
    Drying Processes and Particle Technology in CMC
    Novo Nordisk A / S
    Associate Scientist - I, Formulation Sciences
    MedImmune Inc
    President
    Ellab Inc
    President
    Millrock Technology, Inc.
    Professor University of Geneva, Chairman & CEO, Therapeomic Inc.
    University Of Geneva
    Senior Research Investigator
    BMS
    Managing Director
    Explicat Pharma GmbH
    Director of Technical Sales
    SP Scientific
    Senior Statistician
    Arlenda
    Technical Fellow, Global Manufacturing Science and Technology
    One 2 One Hospira
    CSO
    Xstalbio Ltd
    Engineer I, Pharmaceutical Processing and Technology Development
    Genentech, Inc.
    Principal Scientist
    Momenta Pharmaceuticals Inc
    Director of R&D
    BioPharma Technology
    Research Associate III
    Baxter Pharmaceutical Solutions, LLC
    Project Manager, Global Technology Transfer
    Baxter BioScience

    Sponsors and Exhibitors

    Official Media Partner

    Supporters

    Workshops

    The application of QbD to Freeze-Drying

    The application of QbD to Freeze-Drying

    Renaissance Woodbridge Hotel
    1 May 2015
    Iselin, USA

    Lyophilisation & Freeze Drying USA: Snap shot of confirmed attendees

    Download

    An interview with industry leaders and Lyophilisation USA sponsor/speaker - Millrock Technology

    Download

    SMi presents it’s global Lyophilisation series for 2015

    Download

    Lyophilisation & Freeze Drying USA: An academic perspective from De Montfort University

    Download

    An interview with Ronald Pate, PDS Scientist & Lyophilization Specialist, Patheon Pharmaceuticals Inc.

    Download

    Sponsors and Exhibitors


    Ellab

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

    Ellab is an industry leading manufacturer of wireless dataloggers and wired thermocouple validation systems used in the pharmaceutical industry. Outside of temperature sensors Ellab offers vacuum, pressure, CO2, and RH sensors. Specifically, for the lyophilization process, Ellab specializes in analyzing shelf and product temperatures within a full lyophilization cycle.


    EnWave Corporation

    Sponsors and Exhibitors
    http://www.enwave.net

    EnWave Corporation offers a technology alternative to lyophilization. Radiant Energy Vacuum (REV) technology uses microwave energy under vacuum to homogeneously remove moisture from biopharmaceuticals at lyophilization temperatures and pressures. REV is proven to reduce cycle times dramatically and yield equivalent results to lyophilization, but with significantly less associated capital and operating costs.


    Lyophilization Technology, Inc

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

    Lyophilization Technology, Inc. is a Contract Development and Manufacturing Organization. The company conducts applied research, provides comprehensive scientific services and technical support ranging from developing new freeze dried products and processes, streamlining operations to improving compliance, and manufactures clinical supplies for freeze dried pharmaceuticals, biologics, diagnostics, biopharmaceuticals and fine chemicals.


    MILLROCK TECHNOLOGY

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

    Millrock Technology is a leader in the innovation, design and manufacturing of freeze drying / lyophilization solutions. Since the 1950s, the Millrock team has been solely focused on advancing the science of freeze drying / lyophilization for the pharmaceutical, biotech and related industries, working in partnership with our customers to innovate products that deliver performance and optimize their processes.


    One 2 One

    Sponsors and Exhibitors
    http://www.one2onecmo.com

    One 2 One™ is a global leader in sterile injectables contract manufacturing. We carefully guide your medicine from development through launch, harnessing 25+ years of expertise in biopharmaceutical fill and finish. Organizational strengths include in-depth experience with complex biologics and a lyophilization center of excellence.


    SP Scientific

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

    SP Scientific, leaders in freeze drying innovation, invites you to speak with a representative to learn more about how ControLyo™ Technology, available for pilot to production scale lyophilizers, has improved the freeze-drying industry. Ask about retrofitting your existing unit with ControLyo™ Technology.


    Tempris

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

    iQ-mobil is the developer and manufacturer of the wireless and battery-free temperature measurement system Tempris. Tempris is used for real-time product temperature monitoring and controlling during lyophilization in order to optimize processes and make pharmaceutical production more cost-efficient. Tempris is a PAT-tool and available for all types of freeze dryers according to cGMP guidelines.

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    http://www.cobioscience.com/

    As champions for life science in our state, Colorado BioScience Association leads expansion policies to advance the industry and accelerate growth. We support a thriving bioscience sector by connecting innovators to funding, infrastructure, research and talent. CBSA fosters bioscience workforce and leadership development through opportunities for networking and professional education.


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    Official Media Partner
    http://ondrugdelivery.com

    ONdrugDelivery provides 30,000 readers throughout global pharma/biopharma, with the latest, most pertinent industry information and intelligence about the drug delivery-related ideas, technologies, services and products the sector is developing. Established in 2004, and trusted throughout the industry for its high quality contributions from leading drug delivery experts, ONdrugDelivery is a must for pharma / biotech industry professionals who need to know what’s going on in drug delivery. Subscribe online today to the print or free digital edition: www.ondrugdelivery.com/subscribe.


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    The Protein Society is an international, trans-disciplinary community of investigators dedicated to the study of protein structure, function, and design. A non-profit scientific and educational organization, the Society provides forums for scientific collaboration and communication with respect to all aspects of protein science.

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    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.


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    Pharma Marketing News is an independent monthly electronic newsletter focused on issues of importance to pharmaceutical marketing executives. It is a service of the Pharma Marketing Network -- The First Forum for Pharmaceutical Marketing Experts -- which brings together pharmaceutical marketing professionals from manufacturers, communications companies, and marketing service providers for wide ranging discussions and education on a multitude of current topics. Pharma Marketing Network & Pharma Marketing News provide executive-level content coupled with permission-based e-marketing opportunities.


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    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.


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    Established in October 2003, PharmiWeb Solutions is an energetic, innovative provider of web-based solutions for the pharmaceutical sector, with customers such as AstraZeneca, Roche, Servier Laboratories, and Merck With solutions in three key areas: Online Publishing, e-Business and Mobile Computing, we deliver connectivity – between people and applications – unlocking islands of data and knowledge. We own some of the sector’s most innovative Online Publications: PharmiWeb.com, HospitalPharma.com and Detail-Direct.com. We are actively developing solutions for Mobile Computing platforms. For example, our PharmiTabTM e-pharmacy solution runs real-time patient data and prescribing transactions in a busy hospital environment, on a TabletPC, wireless client/server platform. e-Business solutions range from e-Detailing, to Online Market Research, all designed to increase reach, increase sales, and to reduce administration and costs.


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    Cutting Edge Information provides customized research and benchmarking reports to pharmaceutical, biotechnology and other life science companies. We provide off-the-shelf and customized research for key areas including medical affairs, clinical development, market access, regulatory affairs, marketing management, sales and HCP fair market value.


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    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.


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    MedNous is a print publication and website about medical innovation in Europe. It carries exclusive interviews with companies that are at the forefront of medical technology, as well as contributor articles from prominent practitioners. Our mission is to identify significant advances in medicine and to explain how this innovation is being commercialised. In doing so, we talk to venture capitalists about what products and platforms they are supporting. We report on how regulators cope with the accelerating pace of innovation. And we regularly cover the latest developments in the discovery and development of new medical concepts in the area of antibodies, vaccines, small molecules, regenerative medicine and nanomedicines. MedNous combines the English word for medicine with the Greek word for intellect. And those with nous are readers of our publication. Visit our website: www.mednous.com


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    PharmaCircle is an innovative knowledge management company serving the current and future global leaders in the Pharmaceutical and Biotechnology related industries. PharmaCircle is a one stop information and analysis source for pipeline, products, clinical trials, drug delivery technologies, deals and acquisitions, company financials, venture capital investments, product sales, pharmaceutical services, news, patents and more….


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    CanBiotech - A Portal and B2B Outsourcing Marketplace for the Biotech and Pharmaceutical Industry. The Marketplace features the Outsourcing Services Showcase; the Portal features our biopharmaceutical and venture capital directories and databases. Publications include the BioMedical Outsourcing Report and the Bio Outsourcing Asia© Publication.

    Renaissance Woodbridge Hotel

    515 US Highway 1 South
    Iselin 08830
    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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