- Todos > Medicine Information and Evidence for Policy > Information and Publications
- Todos > Quality and Safety: Medicines > Counterfeit Medicines
- Todos > Quality and Safety: Medicines > International Nonproprietary Names
- Todos > Quality and Safety: Medicines > Quality Assurance
- Todos > Quality and Safety: Medicines > Regulatory Support
- Todos > Quality and Safety: Medicines > Safety and Efficacy
- Todos > Quality and Safety: Medicines > The International Pharmacopoeia
- Todos > WHO Prequalification of Medical Products > WHO-UNICEF-UN Project
- Palabras clave > efficacy and safety of medicines
- Palabras clave > International Nonproprietary Names (INN)
- Palabras clave > International Pharmacopoeia (The)
- Palabras clave > Model Quality Assurance System (MQAS)
- Palabras clave > Prequalification of Medicines Programme - WHO
- Palabras clave > quality assurance
- Palabras clave > registration - Collaborative Registration Procedure (CRP)
- Palabras clave > regulatory matters
- Palabras clave > WHO/PQP and NMRAs - collaborative procedure
(2013; 136 pages)
The fourth issue for 2013 opens with a feature article describing the Collaborative Registration Procedure for WHO-prequalified products and how this accelerates registration through improved information sharing between the WHO Prequalification of Medicines Programme and national medicines regulatory authorities.
The following section, on Quality Assurance of Medicines, presents a review of the MQAS and describes development of the harmonized assessment tool for procurement agencies. In October 2013, the revised MQAS, the assessment tool, Aide Memoire, format for an inspection report, interpretation guideline and the self-inspection tool were adopted by the WHO Expert Committee on Specifications for Pharmaceutical Preparations.
The section on Safety and Efficacy highlights information on signals and reports of adverse drug reactions, with other news from around the world, including labelling changes. This is complemented by the section on Regulatory Action and News which provides information on recent developments from regulatory authorities, and particularly those having an impact on decision-making and risk assessment.
Recent Publications, Information and Events provides information and brief summaries of several recently-published documents and online resources.
The Consultation Documents section presents draft International Pharmacopoeia monographs for comment. They cover several proposals including: Dissolution testing of tablets and capsules; General monograph on parenteral preparations.Test for bacterial endotoxins; Niclosamide, anhydrous and monohydrate; Niclosamide tablets; Sulfamethoxazole and trimethoprim intravenous infusion; Medroxyprogesterone acetate; Fluconazole; Fluconazole capsules; and Fluconazole injection.
The journal concludes with the Proposed International Nonproprietary Names (INN) List 110.