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Resources

Topic
All Analytics Antibody-drug conjugates Bioanalytics Biologics Biosimilars Biostatistics Cancer Cell culture Clinical trials Contamination Drug development Drug product Drug substance EMA FDA GMP Mabion Manufacturing Microbiology Partnership Proteins Regulatory Vaccines Veterinary biologics
Type
All Poster
end-to-end manufacturing of biosimilars

End-to-End Manufacturing of Biosimilars – From Cell Line to Commercial Product 

Biosimilars, Manufacturing
microbiological cleaning in cleanrooms

Microbiological Cleaning in Cleanrooms in CDMO Operation

GMP, Microbiology
Rapid Microbiological Methods (RMMs) enhance sterile drug quality control

Rapid Microbiological Methods in Quality Control of Sterile Drugs

Contamination, Drug product, Microbiology
Analytical Lifecycle for Monoclonal Antibodies

From Research to Release: Mapping Mabion’s Full Analytical Lifecycle for Monoclonal Antibodies 

Analytics, Mabion, Monoclonal antibody

The New Era of Biosimilar Development: Seizing the Opportunity Under EMA’s Streamlined Guidelines

Biosimilars, Clinical trials, Drug development, EMA, FDA, Mabion, Regulatory
downstream development

The Role of Downstream Development in Ensuring Biologic Product Purity and Quality

Drug product, Manufacturing
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Contact

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bd@mabion.eu

Mabion

gen. Mariana Langiewicza 60
95-050 Konstantynów Łódzki
Poland

+48 42 207 78 90

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