About the Workshop:
Regulations direct drug product manufacturers to exclude foreign matter and minimize foreign particle content. Particles can originate from the environment, packaging materials, formulation ingredients, interactions between product and packaging, or be inherent to the product. For inherent species, or the expected formulation-related particle species, which techniques may be most appropriate? This workshop will be a forum for discussing the control and determination of undesired visible and sub-visible particulate matter and also characterization of inherent particle species in biopharmaceuticals.
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Why Attend:
- Gain insight into the USP standard process and how to work with USP to impact future standards.
- Obtain feedback about the current chapters and where gaps exist for future standard work.
- Identify areas where USP can broaden our scope in the biologics space
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Registration:
Click the button below to register today:
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Who should Attend:
- Analytical chemists and biologists
- QA/QC analysts
- R&D scientists, managers
- Manufacturing scientists, managers
- Regulatory affairs specialists
- Contract research organizations
- Contract manufacturing organizations
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Questions:
Email :conferences@usp.org
Phone +1 301-816-8130
Website : www.usp.org/workshops
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