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Croda Pharma Ask the Expert
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Lonza Ask the Expert
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Key strategies for effective technology evaluationKey strategies for effective
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Post-pandemic dip: Panelists discuss CGT challengesPost-pandemic dip: Panelists
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Webcasts
Talent dearth continues to puzzle life sciences industry, says recruitment
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during a video interview at Biotech Week Boston (BWB).

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Experts call for better analytics, customization, R&D, and strategic investments
as cell and gene therapies struggle with funding challenges and complex
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Facilities & CapacityBIOSECURE: China’s loss could be India’s gain

Aurigene’s chief commercial officer says his firm and other Indian CDMOs are “a
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Therapeutic ClassHow and why AstraZeneca’s oncology eyes turned to cell
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Cell therapies will play an increasingly important position in AstraZeneca’s
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Information Technology
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Keys to Successful Technology Transfer

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Emerging Therapeutics
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As the monoclonal-antibody (mAb) market continues to grow, it is becoming
increasingly important for pharmaceutical and biotech companies to accelerate
process development and establish a scalable manufacturing process capable of
achieving high titers and consistent product quality. Central to this is a cell
culture media and feed system that can provide the required nutrients for
optimal cell growth, viability, and function, as well as facilitate a seamless
transition from development to clinical and commercial manufacturing. However,
choosing an appropriate system can be a complex and time-consuming process,
often requiring the evaluation of multiple medium and feed options. Platform
systems, consisting of a medium and complementary feed developed for a specific
cell line and application, have emerged as a valuable option for developers to
help simplify selection and increase scale-up efficiency. To meet the need for
high-performance platform mAb manufacturing solutions, Thermo Fisher Scientific
has dev...

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From Pipettes to Infusion Pumps: Volume Accuracy in Regulated Industries and Its
Critical ImpactFrom Pipettes to Infusion Pumps: Volume Accuracy in Regulated
Industries and Its Critical Impact

Precision in volume delivery is critically important for both the
biopharmaceutical and medical device industries. This special report discusses
how accurate volume measurement affects patient safety, product quality, and
regulatory compliance. Sartorius emphasizes the roles that infusion pumps,
laboratory pipettes, and quality control (QC) measures play in ensuring reliable
and reproducible results. Register or Login and hit Download Now to get the full
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This webcast features: Michael Rauscher, MS, associate principal scientist,
process R&D enabling technologies, Merck & Co., Inc. Multimodal chromatography
has a history of providing value for biopharmaceutical separations. Ligands that
enable binding based on both charge and hydrophobic interactions provide more
opportunity for effective separation of multiple product- and process-related
impurities. However, more diverse protein therapeutics and evolving expression
systems present separation challenges that may not be easily addressed by
commercially available multimodal resins. As an alternative to current
multimodal anion exchange (MMAEX) resins with quaternary ammonium groups,
Bio-Rad’s new Nuvia wPrime 2A Resin offering provides MMAEX functionality with a
weak anion exchanger. This webinar will discuss several molecules that were
prioritized for high-throughput evaluation of Nuvia wPrime 2A Resin, including
an IgG1 monoclonal antibody (mAb), IgG4 mAb, and a bispecific antibody (bsAb),
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Purpose

This webcast features: Alla Zilberman, PhD, vice president, technical marketing
, Cygnus Technologies. Antibody Affinity Extraction (AAE) is a powerful
orthogonal approach to determine if a host cell protein (HCP) ELISA is fit for
purpose. AAE is referenced as immunoaffinity chromatography in USP 1132 and has
been used in over 300 projects to perform antibody coverage analysis for
regulatory submissions. This webinar focuses on several case studies
demonstrating utility of AAE-MS method in identification of immunoreactive HCPs
to establish HCP antibody coverage, HCPs enriched during process changes, and
HCPs co-purified with DS. Thank you for your interest in this webcast. You may
submit your request to view the webcast, and you will receive a confirmation
email with log-in details.

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Sustainability in Life Sciences: Actionable Solutions for Improving Energy
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Formulations and Drug-Device Combination Products

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Process Control) for CHO Fed-Batch Application
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Process Control) for CHO Fed-Batch Application



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Platform
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