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Pharmaceutical Regulatory Environment - Al-Essa, Reem K.

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        Présentation Pharmaceutical Regulatory Environment de Al - Essa, Reem K. Format Broché

         - Livre Médecine, Pharmacie, Paramédical, Médecine vétérinaire

        Livre Médecine, Pharmacie, Paramédical, Médecine vétérinaire - Al-Essa, Reem K. - 01/10/2016 - Broché - Langue : Anglais

        . .

      • Auteur(s) : Al-Essa, Reem K. - Salek, Sam - Walker, Stuart - Al-Rubaie, Mohammed
      • Editeur : Springer International Publishing Ag
      • Langue : Anglais
      • Parution : 01/10/2016
      • Format : Moyen, de 350g à 1kg
      • Nombre de pages : 252
      • Expédition : 388
      • Dimensions : 23.5 x 15.5 x 1.4
      • ISBN : 9783319360102



      • Résumé :

        Reem Al-Essa BPharm MSc PhD was the Drug Registration and Release Superintendent for six years of her 12 years experience with?Ministry of Health, Kuwait. During this period she completed her MBA with distinction. She later undertook the EU2P MSc in Pharmacovigilance and Pharmacoepidemiology. Dr Al-Essa has published six journal articles and abstracts related to pharmaceutical regulation in the Gulf region.

        Mohammed?Hamdan?Al-Rubaie?BPharm?MSc PhD is the Director of Drug Control, Directorate?General?of Pharmaceutical?affairs and?Drug Control, Oman Ministry of Health.He is a member of the GCC Central Registration Committee, and actively involved in many other GCC committees and working groups for the?drafting?of the?GCC pharmaceutical regulations and policies. Dr Al-Rubaie?was instrumental in forming the Pharmaceutical?society?in Oman and chaired it from 2010-2011.

        Stuart WalkerBSc, PhD, MFPM FRSC FIBiol, FRCPath , is the Founder of the Centre for Medicines Research International, the Centre for Innovation in Regulatory Science and Professor of Pharmaceutical Medicine, University of Wales, Cardiff. During his research career in academia & industry, he has supervised many PhD programmes in clinical development, regulatory policies, the benefit/risk assessment of medicines and health technology assessment, co-authored 280 research papers and edited 25 books. He is frequently involved in the organisation of international meetings on key issues that concern the regulatory review of medicines and has lectured extensively throughout Europe, the USA, the Asia-Pacific Region, Latin America and the Middle East.

        Sam Salek PhD RPh FFPM MRPSGB MCMS FESCP is Professor of Pharmacoepidemiology at the University of Hertfordshire, Hatfield, visiting Professor at the Estate of Hessen, Germany, and Director of the Institute for Medicines Development, Cardiff, UK. Professor Salek's research focuses mainly on four areas: development and application of patient-reported outcome measures...

        Biographie:
        Reem Al-Essa BPharm MSc PhD was the Drug Registration and Release Superintendent for six years of her 12 years experience with Ministry of Health, Kuwait. During this period she completed her MBA with distinction. She later undertook the EU2P MSc in Pharmacovigilance and Pharmacoepidemiology. Dr Al-Essa has published six journal articles and abstracts related to pharmaceutical regulation in the Gulf region.Mohammed Hamdan Al-Rubaie BPharm MSc PhD is the Director of Drug Control, Directorate General of Pharmaceutical affairs and Drug Control, Oman Ministry of Health.He is a member of the GCC Central Registration Committee, and actively involved in many other GCC committees and working groups for the drafting of the GCC pharmaceutical regulations and policies. Dr Al-Rubaie was instrumental in forming the Pharmaceutical society in Oman and chaired it from 2010-2011. Stuart Walker BSc, PhD, MFPM FRSC FIBiol, FRCPath, is the Founder of the Centre for Medicines Research International, the Centre for Innovation in Regulatory Science and Professor of Pharmaceutical Medicine, University of Wales, Cardiff. During his research career in academia & industry, he has supervised many PhD programmes in clinical development, regulatory policies, the benefit/risk assessment of medicines and health technology assessment, co-authored 280 research papers and edited 25 books. He is frequently involved in the organisation of international meetings on key issues that concern the regulatory review of medicines and has lectured extensively throughout Europe, the USA, the Asia-Pacific Region, Latin America and the Middle East. Sam Salek PhD RPh FFPM MRPSGB MCMS FESCP is Professor of Pharmacoepidemiology at the University of Hertfordshire, Hatfield, visiting Professor at the Estate of Hessen, Germany, and Director of the Institute for Medicines Development, Cardiff, UK. Professor Salek's research focuses mainly on four areas: development and application of patient-reported outcome measures...

        Sommaire:
        drug safety evaluation and pharmacovigilance...

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