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65 documents on 2 pages
 
 
 
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2nd Biennial Scientific Conference on Medicines Regulation in Africa. Addis Ababa, Ethiopia, 30th November to 1st December 2015 - Book of Abstracts. Conference Theme: Regulatory Systems Strengthening for advancing Research, Innovation and Local Pharmaceutical Production in Africa

Year:

2015;

Pages:

38;


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Addressing the Barriers to Effective Monitoring, Reporting and Containment of Spurious/Substandard/Falsely-labelled/ Falsified/Counterfeit Medical Products through Sustainable Multi-stakeholder Collaboration and Community/Consumer-based Interventions. A report prepared for the Medicines Transparency Alliance, Philippines

Year:

2016;

Pages:

94;


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Compendium of Good Manufacturing Practices (GMP) Technical Documents for Harmonization of Medicines Regulation in The East African Community, 2014

Year:

2014;

Pages:

336;


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Compendium of Medicines Evaluation and Registration for Medicine Regulation Harmonization in The East African Community, 2014

Year:

2014;

Pages:

312;


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Drug Registration Guidance 2073. (Issued under Drug Registration Regulation 2038). MOH, Nepal, 2016

Year:

2016;

Pages:

177;


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First Biennial Scientific Conference on Medicines Regulation in Africa. Johannesburg, Afrique du Sud, 2–3 December 2013 - Book of Abstracts. Conference Theme: Building Partnerships for Sustainable Capacity Development in Medicines Regulation in Africa [French]

Year:

2013;

Pages:

72;


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First Biennial Scientific Conference on Medicines Regulation in Africa. Johannesburg, South Africa, 2-3 December, 2013 - Conference Report. Conference Theme: Building Partnerships for Sustainable Capacity Development in Medicines Regulation in Africa

Year:

2013;

Pages:

84;


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Guideline for Registration of Medicines. Third Edition, June 2014 - Ethiopia

Year:

2014;

Pages:

141;


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Guidelines for Medicinal Product Registration - Sierra Leone

Year:

2013;

Pages:

28;


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Industrial Perceptions of Medicines Regulatory Harmonization in the East African Community

Year:

2019;

Pages:

15;

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Lignes directrices pour la préparation et la soumission de dossiers en format document technique commun. Septembre 2015 - République démocratique du Congo

Year:

2015;

Pages:

33;


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Lignes directrices relatives a l’homologation des médicaments à base des plantes. Septembre 2015 - République démocratique du Congo

Year:

2015;

Pages:

18;


 
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Lignes directrices relatives au dépôt des demandes d’enregistrement au format CTD (common technical document) : qualité. Septembre 2015 - République démocratique du Congo

Year:

2015;

Pages:

62;


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MOH Guidelines on Submission of Documentation for Registration of Human Pharmaceutical Products. First Edition, 2014 - Republic of Rwanda

Year:

2014;

Pages:

436;


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Première Conférence Scientifique Biennale sur la Réglementation des Médicaments en Afrique. Johannesburg, Afrique du Sud, 2-3 Décembre 2013 - Livre des Résumés. Thème de la Conférence : Établir des Partenariats pour le Renforcement Durable des Capacités dans la Réglementation des Médicaments en Afrique [English]

Year:

2013;

Pages:

70;


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Quality and Safety of HIV/AIDS Medicines in Namibia October 2015-September 2016

Year:

2016;

Pages:

18;


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Rapid Evaluation of the Medicines Registration System in Benin. November 2016

Year:

2016;

Pages:

24;


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Registration and Quality Assurance of ARVs & Other Essential Medicines in Namibia. October 2014 - September 2015

Year:

2015;

Pages:

21;


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Report of the Second Meeting of the Member State Mechanism on Substandard/spurious/falsely-labelled/falsified/counterfeit Medical Products. (A/MSM/2/6)

Year:

2013;

Pages:

11;


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Règlement N° 06/2010/CM/UEMOA relatif aux procédures d’homologation des produits pharmaceutiques à usage humain dans les états membres de l’UEMOA

Year:

2010;

Pages:

12;


 
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SIAPS’ Technical Assistance to Strengthen Medicines Regulation in Namibia: 2011–2017. December 2017

Year:

2017;

Pages:

33;


Countries:

 
 
 
 
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