Strategy for Pooled Procurement of Essential Medicines and
Health Commodities, 2013-2017
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Quality assurance
The quality assurance of pharmaceutical products is a wide-ranging
concept that covers all matters that individually or collectively influence
the quality of a product. It is the totality of the arrangements made to
ensure that pharmaceutical products are of the quality required for their
intended use.
Quality control
The quality control of pharmaceutical products is a concept that covers
all measures taken—including the setting of specifications, sampling,
testing and analytical clearance—to ensure that the raw materials,
intermediates, packaging materials and finished pharmaceutical
products conform with established specifications for identity, strength,
purity and other characteristics.
Tracer medicines
Medicines selected by the surveyors in the 2010 Pharmaceutical
Marketing Analysis study, of which the assembled data form the baseline
for measuring implementation of the Strategy.
Standardisation
Standardisation is the process of establishing a technical standard,
which could be a standard specification, standard test method,
standard definition, or standard procedure. Standardisation means that
there is a standard specification, unit, instruction or characteristic that is
understood globally.
Work sharing
The sharing of “good practices”, as laid down in guidelines, standard
operating procedures (SOPs), standard bidding documents, tender
adjudication reports, storage conditions, distribution schedules, etc.
See http://www.who.int/trade/glossary/story078/en/index.html [accessed 4 April 2013]
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