Oxford Global Formulation and Drug Delivery Congress 2014 London

  • Conference Call
  • Oxford Global Con­fer­ences are proud to present the For­mu­la­tion & Drug Deliv­ery Con­gress, tak­ing place on 2 – 3 Octo­ber 2014 in Lon­don, United King­dom.

    New drug deliv­ery part­ner­ships, advances in for­mu­la­tion tech­nolo­gies and sig­nif­i­cant improve­ments in analy­sis capa­bil­i­ties are all cre­at­ing real oppor­tu­ni­ties in the prod­uct devel­op­ment field. This senior level con­gress brings together over 150 experts work­ing in for­mu­la­tion, deliv­ery and prod­uct devel­op­ment. Pre­sen­ta­tions will assess recent tech­no­log­i­cal inno­va­tions and dis­cuss their impact on prod­uct improve­ment and patient experience.

    Day One of the Con­gress will cover meth­ods to improve sta­bil­ity and bioavail­abil­ity. Speak­ers will dis­cuss the lat­est tech­nolo­gies being employed in crys­tal engi­neer­ing, par­ti­cle size reduc­tion and self emul­si­fi­ca­tion. Experts will also com­pare meth­ods for char­ac­ter­is­ing drug deliv­ery action and debate novel solu­tions for dif­fi­cult to deliver drugs.

    Day Two will look at the lat­est advances in process and prod­uct devel­op­ment. Pre­sen­ta­tions will cover con­tin­u­ous man­u­fac­tur­ing, clin­i­cal prod­uct test­ing and Qual­ity by Design ini­tia­tives. The pro­gramme will also cover ways of ensur­ing prod­uct qual­ity ear­lier in the pipeline, through pre-​formulation strat­egy and early stage inter­ven­tions. Day Two also fea­tures a ded­i­cated Bio­pharma stream, explor­ing the role of nan­otech­nolo­gies, HT method­olo­gies and early devel­opa­bil­ity screens in the for­mu­la­tion and deliv­ery of biologics.

    Agenda

    In keep­ing with Oxford Global’s highly suc­cess­ful life sci­ences series, an expert panel of 40 speak­ers will present a full con­fer­ence pro­gramme cov­er­ing the top­ics out­lined below.

    Day 1

    Opti­mis­ing Formulation

    • Opti­mis­ing for­mu­la­tion: improv­ing sta­bil­ity and bioavailability
    • De-​risking for­mu­la­tion strat­egy: IVIVC, pre­dic­tive mod­el­ling, early screen­ing, excip­i­ent com­pat­i­bil­ity testing
    • Advances in for­mu­la­tion test­ing: sta­bil­ity sim­u­la­tion test­ing, dis­so­lu­tion testing
    • Novel tech­nolo­gies: self-​emulsifying tech­nol­ogy, microformulations
    • Improv­ing sol­u­bil­ity: crys­tal engi­neer­ing, solid dis­per­sion, par­ti­cle size reduc­tion, hot melt extrusion

    Improv­ing Drug Delivery

    • Enhanc­ing drug effi­cacy from deliv­ery: par­enteral deliv­ery, long-​acting formulations
    • Char­ac­ter­is­ing drug deliv­ery action: imag­ing, par­ti­cle size analysis
    • Dif­fi­cult to deliver drugs: poorly sol­u­ble drugs, age appro­pri­ate delivery
    • The increas­ing role of nan­otech­nol­ogy in drug delivery
    • Drug deliv­ery case stud­ies: trans­der­mal, sublingual

    Day 2

    For­mu­la­tion and Drug Deliv­ery Strate­gies for Biopharma

    • Pre-​formulation activ­i­ties for bio­log­ics: pre­dict­ing pro­tein behav­iour, early screen­ing for developability
    • Opti­mis­ing bio­log­ics for­mu­la­tion: improv­ing qual­ity and stability
    • For­mu­lat­ing high con­cen­tra­tion and high strength proteins
    • For­mu­la­tion and deliv­ery chal­lenges for novel bio­log­i­cal drug formats
    • New tech­nol­ogy case stud­ies: nan­otech­nol­ogy, HT methodologies
    • Biosim­i­lar for­mu­la­tion and delivery

    Prod­uct Devel­op­ment Considerations

    • User-​focused prod­uct devel­op­ment: what do patients need from admin­is­tra­tion systems?
    • Imple­ment­ing Qual­ity by Design from pre-​formulation through to com­mer­cial manufacture
    • Man­ag­ing exter­nal stake­hold­ers: work­ing with CROs, CMOs and reg­u­la­tors to cre­ate the opti­mal deliv­ery system
    • Tech­nol­ogy and process trans­fer: from for­mu­la­tion research to suc­cess­ful prod­uct launch

    2014 Speakers

    • Sreed­hara Alavat­tam – Senior Scientist/​Senior Group Leader, Late Stage Phar­ma­ceu­ti­cal Devel­op­ment, Genentech
    • Anne Bechet – Direc­tor Project Man­age­ment, Prosensa
    • Steve Brown – Exec­u­tive Direc­tor, Phar­ma­ceu­ti­cal Tech­nol­ogy, Actavis
    • Paul Dalby – Pro­fes­sor of Bio­chem­i­cal Engi­neer­ing and Biotech­nol­ogy, UCL
    • Den­nis Douroumis – Direc­tor of Cen­tre for Inno­va­tion in Process Engi­neer­ing and Research (CIPER), Board Mem­ber of the Acad­emy of Phar­ma­ceu­ti­cal Sci­ences (APS), Reader in Phar­ma­ceu­ti­cal Sci­ences, Uni­ver­sity of Greenwich
    • David Haase – Senior Man­ager Device Devel­op­ment, Genentech
    • Sune Klint Ander­sen – Prin­ci­pal Sci­en­tist Dry­ing Processes, Novo Nordisk
    • Jayne Lawrence – Pro­fes­sor of Bio­phys­i­cal Phar­ma­ceu­tics, King’s College
    • Ulrik Lytt Rah­bek – Direc­tor, Head of ADME Depart­ment, Dia­betes Research, Novo Nordisk
    • Sachin Mit­tal – Direc­tor, Merck
    • Ric­cardo Pan­icucci – Global Head of Chem­i­cal & Phar­ma­ceu­ti­cal Pro­fil­ing (CPP), Novar­tis Insti­tutes for Bio­Med­ical Research, Inc.
    • Bernardo Perez-​Ramirez – Senior Sci­en­tific Direc­tor, Bio­For­mu­la­tions Devel­op­ment, Gen­zyme Corporation
    • Harpreet Sandhu – Prin­ci­pal Sci­en­tist, Merck
    • Yun Tang – Senior Man­ager, Ana­lyt­i­cal Oper­a­tions, Genentech
    • Thorsten Thor­mann – Senior Vice Pres­i­dent, LEO Pharma
    • Sal­vador Ven­tura – Full Pro­fes­sor, Pro­tein Fold­ing and Con­for­ma­tional Dis­eases Lab (PFCD), Uni­ver­si­tat Autònoma de Barcelona
    • Mark Wil­son – Direc­tor, Col­lab­o­ra­tion Man­age­ment, Europe, Plat­form Tech­nol­ogy and Sci­ence, GSK
    • Mark Yang – Direc­tor, Fill Fin­ish Devel­op­ment, Late Stage Process Devel­op­ment, Gen­zyme, A Sanofi Company
    • Matthew Yates – Direc­tor, Eli Lilly

    Sub­mit a poster

    For atten­dees inter­ested in sub­mit­ting a poster, there are oppor­tu­ni­ties now avail­able. Your poster pre­sen­ta­tion will be located in the exhi­bi­tion room for two days along­side other posters from senior sci­en­tists work­ing in indus­try and academia.

    We will require:

    Poster title, Abstract (200 words or less)
    Prin­ci­pal author, Organ­i­sa­tion
    Mail­ing address, Email, Tele­phone, Fax
    Addi­tional authors

    In order to secure your board space a fee of £250 will be required. The poster should be pre­sented as A0 (841mm x 1189mm) por­trait size.

    To take advan­tage of this oppor­tu­nity you need to be reg­is­tered as a paid del­e­gate over the 2 days. We have lim­ited spaces avail­able, so please reg­is­ter soon.

    Who will attend

    The For­mu­la­tion & Drug Deliv­ery Con­gress is an exclu­sive event designed for senior level atten­dees from lead­ing phar­ma­ceu­ti­cal, bio­phar­ma­ceu­ti­cal, biotech­nol­ogy, diag­nos­tics, CRO and solu­tion provider com­pa­nies, along with highly esteemed mem­bers of aca­d­e­mic and gov­ern­ment institutions.

    Del­e­gates typ­i­cally include VPs, Direc­tors and Global Heads of:

    • Admin­is­tra­tion systems
    • Bio­man­u­fac­tur­ing
    • Bio­pro­cess­ing
    • CMC
    • Deliv­ery devices
    • Drug deliv­ery
    • For­mu­la­tion for biologics
    • For­mu­la­tion technology
    • Life­cy­cle management
    • Man­u­fac­tur­ing
    • Nan­otech­nol­ogy
    • Pre-​formulation strategies
    • Process improve­ment
    • Prod­uct characterisation
    • Prod­uct development
    • Prod­uct formulation
    • Prod­uct testing
    • Qual­ity By Design
    • Sta­bil­ity testing
    • Tech­nol­ogy development
    starting: ending: 03.10.2014 Location: , Category:

    Timeline

    Conference START 03.10.2014 END

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