This interactive roundtable brought together industry experts to explore the unique challenges of outsourcing peptide drug development with CDMOs and CMOs. The conversation highlights critical pain points across the development journey, including: - Synthesis & Scale-Up: The technical complexity of moving from lab-scale peptide synthesis to commercial volumes while managing yield, purity, and cost. -...

The optimization of cell culture media is a critical factor in achieving efficient and reliable vaccine production. Among the key components, peptones have demonstrated significant potential in enhancing cell growth, viability, and productivity. In this webinar, we will explore the impact of peptones on vaccine manufacturing, with a focus on their role in improving performance...

In addition to basic chemicals and formulation, there are other criteria that contribute to making something an effective and optimal sporicide. The requirements for selecting an agent or replacing an existing sporicide for use within the clean room facility should consider several key factors. This webinar, presented by Professor Tim Sandle, PhD in partnership with...

In an era of rapid disruption and technological advancement, clinical operations leaders face mounting pressure to deliver greater effectiveness while navigating complex trade-offs. This webinar explores how organizations are rethinking their clinical operating models—balancing innovation, efficiency, and strategic decision-making. Join industry experts as we unpack the latest trends, challenges, and opportunities shaping the future of...

Biologic therapies are transforming healthcare, but their complexity brings unique challenges for downstream quality control (QC). Ensuring product purity, safety, and consistency requires precise and reliable analytical methods, especially in the face of regulatory scrutiny. Two critical areas of focus are HPLC protein analytics and residual DNA testing, both of which present technical hurdles that...

Biopharmaceutical development requires a clear understanding of how process conditions affect product quality. For therapeutic antibodies, preserving biological activity—such as antigen binding and effector functions—depends on precise control of cell culture environments. Traditional scale-up metrics like power per volume (P/V), however, often fall short when processes are transferred across facilities or equipment scales. In this...

Join us on Wednesday, November 12th for a forward-looking event exploring the current and next generation of raw materials shaping the mRNA and oligo therapeutics landscapes. This event will bring together industry leaders to discuss advancements in raw materials, including novel enzymes, optimized capping reagents, and other essential materials. We will look at how the...

We are very excited to invite you to the BVS and BioMed Realty Biotech Community Event in Cambridge! Mark your calendars for a great opportunity to connect with industry leaders, explore innovative products, and mingle with fellow professionals in the biotech community. The event will be held at 650 East Kendall Street and all the...

The Regional Biotechnology Conference is an annual conference that attracts more than 100 of the region’s movers and shakers for a half-day of dynamic speakers and topics that are important to start-up and early stage biotech company leaders. This year's conference will feature keynote speakers, Nicholas A. Siciliano, Ph.D., CEO of Vittoria Biotherapeutics. The afternoon...

The minimum-viable-product concept was born not in advanced therapy, but in the tech sector. It asks: What's the smallest set of materials or features required to achieve the desired outcome? This principle can be a powerful guide when sourcing raw materials for gene therapy. Executive Editor Jon O'Connell hosts this Cell & Gene Live event,...