i+academy
- Medicines regulation
- Procurement of antimalarials
- Communication skills
- Systèmes de santé: une présentation
- Brochure
- Essential readings
- Supplier evaluation
- Warehousing and distribution of laboratory commodities
- Recursos humanos
- Further readings
- Basic principles of procurement
- Specific help
- Core readings
- Monitoring and evaluation of supply chain systems
- Quality assurance of medicines in the warehouse
- Fin du cours
- Dia 1. 25 agosto 2015
- Inventory management system
- Evaluating quotations and negotiations
- Assurance qualité des médicaments
- Utilização racional dos medicamentos
- Your assignment for M&E
- Assurance qualité au moment des achats
- Procurement – an overview
- Assurance qualité pendant la distribution
- Annex 8. How to pull the order tracking report for Goods in Transit
- Health systems. An overview
- Strategic and operational management
- Warehousing and distribution
- L'éthique de l'approvisionnement
- Basic principles of medicines procurement
- Recursos humanos para la gestión de la cadena de suministro
- Sanitation and hygiene
- The concept of laboratory commodity security
- Online spell-check
- General introduction
- Warehousing and distribution of laboratory commodities
- La sélection du fournisseur
- Standard operating procedures and working instructions
- Assurer la qualité des médicaments au cours de l'approvisionnement
- Bibliographie
- GMP requirements for documentation
- A functional M&E system to strengthen healthcare
- Introduction to supply chain management
- Burundi
- Finance in the procurement process
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Course catalogue
Free course
Free course
This short introductory course offers basic concepts and exercises on the quantification of medicines and health products.
Upcoming course
Course dates: from 4/03/2019 until 15/04/2019
Duration: 6 weeks
Duration: 6 weeks
i+ Timeline
These dates may be subject to change.
i+ Scholarships
Some of the participants who received a scholarship by i+solutions this year
Nossos participantes
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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
- 5 Feb, 10:50Carole Piriou
- 21 Sep, 10:54Griet Samyn
- 28 Jun, 14:08support user