Feliza Mirasol

A slew of solid-dose drug recalls were issued over the course of 2020 and in early 2021 after nitrosamine contamination was found in products.

Traditional biologic-based testing methods may need an upgrade to properly test newer therapeutic modalities.

Open communication and transparency coupled with technical expertise foster strong long-term manufacturing partnerships.

CDMOs address the unique challenges of liquid and lyophilized forms as well as preparing for the large capacity needed for COVID-19 vaccines.

Traditional biologic-based testing methods may need an upgrade to properly test newer therapeutic modalities.

The number of recommendations for European marketing authorization of human medicines saw significant increase in 2020 over the previous year.

Early detection and more sensitive methods of detecting adventitious agents are becoming increasingly critical in bioprocessing.

The manufacture of gene therapy vectors is shifting to more modern technologies.

The early success seen on the market for approved cell and gene therapies poses both technical and manufacturing challenges for pipeline candidates on the road to commercialization.

Appropriate analytical assays are needed to determine and ensure that biosimilar critical quality parameters are on track.