i+academy
- Exercices pratiques - niveau 2
- Facilitator's space
- Transport and distribution
- Cours de pré-inscription
- Introduction à la gestion de la chaîne d'approvisionnement
- Espacio para el participante
- Product selection
- Garantia de qualidade de medicamentos
- HIV/AIDS: disease and diagnosis
- Introducción a la cadena de suministro de medicamentos
- Introduction to the module
- Exercices pratiques - niveau 3
- Introduction to the alumni course
- Evaluating quotations and negotiations
- SOPs i+academy
- Quality assurance of medicines
- Health systems - an overview
- L'approbation du client et l'attribution du contrat
- Procurement of laboratory commodities
- Importance of quality assurance
- Client approval and contract award
- Suivi et évaluation des systèmes de gestion de la chaîne logistique
- Performance management
- Change management
- Consultancy
- To be considered
- Procurement methods and tender documents
- Discussion forum on health systems and HSS
- Finance in the procurement process
- Systèmes de santé: une présentation
- The development of a M&E work plan for SCM
- Measuring supplier performance
- Principes de base en matière d'achat de médicaments
- Introdução ao ciclo da cadeia de suprimentos medicinais
- Case study Zendalia
- Laboratory services network as part of the health system
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i loved the practical exercises as these gave me a bettter understanding of the course (Paul, Uganda)Ignorar Free course
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Course catalogue
Free course
Free course
This course will equip participants with a basic understanding of the disease malaria, its diagnosis and treatment.
This is a open online course without facilitation.
Novo curso
Datas do curso: desde 27/08/2018 até 8/10/2018
Duração: 6 semanas
Duração: 6 semanas
i+ Timeline
These dates may be subject to change.
Nossos participantes
Verify certificate
Introduza o código do certificado a verificar:
SCM glossary entry
Stringent Regulatory Authorities (SRAs) are national regulatory authorities that apply standards for quality, safety, and efficacy that WHO considers similar to its own. To qualify as an SRA, a country must either be a member of or observer to the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use or have a mutual, legally binding recognition agreement with a member.
Últimos anúncios
- 28 Jun, 14:08support user
- 7 Fev, 21:23Carole Piriou
- 4 Dez, 10:59Carole Piriou