Newsletter | November 30, 2023

11.30.23 -- How To Move mRNA Forward

SPONSOR

Webinar: Practical Applications Of ICH E6(R3): What Do We Need To Do?

Join industry experts December 14 as they discuss the strategic, conceptual, and operational implications of the shift toward risk-based monitoring in the ICH E6(R3) draft guidelines, and what sponsors and vendor partners should already be doing to thrive in the future of clinical trial management. Click here to learn more.

FEATURED EDITORIAL

What We Need To Unlock Next-Generation mRNA Therapeutics

In order to truly unlock the next generation of mRNA therapeutics, we need to think outside the box (and we also need more funding).

INDUSTRY INSIGHTS

SAR – Sequence-Activity Relationships For Efficient Protein Engineering

As protein-based therapeutics gain traction in the greater market, innovative techniques aimed at their optimization have become a key driver for industry.

Establishing Flexibility For Parenteral Cleanroom Manufacturing

Cleanroom systems are purposely designed to simplify the implementation of aseptic manufacturing space needed by the industry to meet future sterile injectable capacity demands.

Advances In Bioprocessing For Biologics And Gene Therapy Vectors

This article collection highlights the importance of continued research and development in the field of bioprocessing to revolutionize the next generation of therapies and personalized medicine.

Contamination Control Technologies And Minimizing Filter Plugging

Learn about the three most common sources of filtration failures and how to prevent these problems.

Assessing Critical Quality Attributes In hiPSCs – Colony Morphology Matters

We explain the differences between high-quality and low-quality colony morphology and how to overcome the challenges of spontaneous differentiation.

How Biopharma Can Address Specialized Skills Gaps And Improve Resilience

Learn how professional training and education programs combined with advanced digital learning technology are key to train local talent and secure biomanufacturing resilience.

CRISPR Clinical Trials And Regulatory Approval Of CRISPR Therapy Drugs

Navigate the intricate regulatory landscape with knowledge that can help you move your CRISPR therapies quickly and efficiently through clinical trials.

Antibody Drug Conjugates And The Global Research Landscape

Learn about ADC advancements in cancer treatment and how the therapy could potentially revolutionize the field by reducing the often-severe side effects associated with traditional chemotherapy.

Cutting Difficult Targets Down To Size

Discover a plasma B discovery workflow that addresses these problems by using cutting-edge single-cell screening technology to revolutionize antibody discovery.

Mitigating Financial Risk Before Selecting An Outsourcing Vendor

Gain insight from several clinical operations experts into the significance of meticulous contract examination when choosing an outsourcing partner to better prepare for these instances.

SPONSOR

Webinar: Cost Efficient Manufacturing Of Purer AAV Gene Therapy Vectors

The goal of AAV downstream process (DSP) is to achieve high recovery of >90% full AAV capsids. The webinar will compare the cation exchange and affinity column. It will also detail how the new CIMmultus HR (high reproducibility) line columns, which include better resolution and narrower acceptance criteria, are used for the polishing step. Click here to learn more.

SOLUTIONS

Cell Therapy Product Characterization Services

Cell Therapy: Streamline The Path From Discovery To Commercialization

Drug Development Strategy Solutions

MicroCNX Series Connectors Specification

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