ArticlesBioPharma December 1, 2023 Democratizing GMP Manufacturing for the New Therapeutic Pipeline PharmTech Europe discusses technology that enables the “democratization” of mRNA manufacturing with... admin-element
ArticlesRegulatory December 1, 2023 Getting your investigational drug regulatory ready Navigating regulatory requirements can be an overwhelming and time-consuming part of the translational... admin-element
Articles December 1, 2023 Insights from process developers – top challenges in recombinant protein purification You might be one of the many process developers who are working on a diversity… admin-element
Articles December 1, 2023 Report from the 6th International HTPD Conference The biggest challenge is still the people and Quantitative Structure-Activity Relationship... admin-element
ArticlesBioPharma November 17, 2023 Developing oligonucleotide therapeutics with confidence In this video, we will look at key considerations for oligo therapeutic developers entering the... admin-element
Articles November 17, 2023 Good modeling practice: workflow and case study Learn more about a recommended mechanistic modeling workflow for successful in silico... admin-element
ArticlesDownstream November 17, 2023 Top challenges in recombinant protein purification process development In this video, Emma Lind, Product Manager for Chromatography Resins at Cytiva answers questions from... admin-element
ArticlesDownstream November 3, 2023 Process Development for Viral Vectors Scaling viral vector processes can be challenging, but it doesn't have to slow you down. admin-element
ArticlesDownstream November 3, 2023 Chromatography processes for the diversified therapeutic antibody pipeline The diversity of antibody variants in today’s pipeline presents unique challenges for purification and we… admin-element
ArticlesBioPharma November 3, 2023 Digitalization: The Route to Biopharma 4.0 Industry 4.0, also known as the Fourth Industrial Revolution (4IR), will result in the digital... admin-element