This symposium brought together stakeholders involved in the manufacture, characterisation and use of reference standards to exchange their views and opinions on the different issues related to the subject. The programme covered the use and establishment of reference standards, including reference standards for new and complex biologicals and small molecules, and regulatory expectations and harmonisation across the regions.
Target audience
This symposium is of interest to professionals from the pharmaceutical industry, regulatory agencies, medicines control laboratories and academic institutions.
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- Session 1: Compendial Reference Standards
- Session 2: Pharmaceutical Reference Standards Small Molecules
- Session 3: Pharmaceutical Reference Standards for biologicals
- Session 4: Regulatory Aspects
Poster Presentations
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