The
European Pharmacopoeia (Ph. Eur.) Commission decided to restructure Section 3.
of the Ph. Eur. on materials and containers. A new Subsection 3.3. has been
added to Section 3. in order to cover specific medical devices: containers for
human blood and blood components, and materials used in their manufacture;
transfusion sets and materials used in their manufacture; syringes.
The
new structure of Section 3. will be published in the 10th Edition of the Ph.
Eur. which will enter into force on 1 January 2020.
Posted by Dr. Tim Sandle,
Pharmaceutical Microbiology
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Pharmaceutical Microbiology