Newsletter | April 8, 2024

04.08.24 -- ICYMI: Q1 2024's Cell & Gene Live And Cell & Gene: The Podcast

SPONSOR

Sequence identity confirmation for genetically modified products is a regulatory expectation. Learn how NGS can add value to your testing program, including sequence through highly complex regions such as GC rich regions or strong secondary structure, and overcome the challenge of obtaining an accurate sequence for the inverted terminal repeats found in adeno-associated virus (AAV) vectors.

FROM THE EDITOR

ICYMI: Q1 2024’s Cell & Gene Live And Cell & Gene: The Podcast

With Q1 of 2024 coming to a close, I wanted to take this opportunity to make sure you’ve read, heard, or viewed some of the insightful content we’ve created for Cell & Gene's readers since the start of the year.

INDUSTRY INSIGHTS

Outsourcing Vendor Red Flag #3: Inaccurate Or Low Bids

A bad feeling in your gut is a firm starting point, but strategies exist to substantiate a bid’s value based on more than the “sniff test.”

Build A Foundation For Successful Clinical Manufacturing

Establishing both the QTPP and CQA for your drug at the beginning of the product life cycle is crucial for a successful GMP manufacturing process.

Key Considerations When Developing Your Combination Product

Succeed in combination product development by understanding the risk factors that may arise and implementing mitigation strategies that will streamline the device development process.

A Mammalian Suspension Technology For Scalable rAAV Production

Explore a HEK293 derived animal component-free suspension cell line as the foundation of an up to 2000-liters scalable and robust platform process that increases the speed of AAV manufacturing.

Put Your AAV On The Fast-Track To The Clinic

Review an innovative approach to fast-tracking AAVs through a platform approach that easily scales as the project progresses to late-stage GMP production and to market.

SOLUTIONS

Supply Chain Challenges For Cell And Gene

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