Crystal Hostler

Jan 10, 2025 | bioprocessonline.com | Tyler Menichiello |Crystal Hostler |Mesa Laboratories |Charlie Wakeham

Let Us Handle Your Buffer PreparationThermo Fisher Scientific is here to support you with the buffer preparation in your manufacturing workflow. Leaving the non-core activities to us enables you to focus on the patient therapy development. Our capabilities cover off-the-shelf products like WFI, NaOH, NaCl, or EtOH, a library of the most frequently used buffers that are made-to-order, as well as fully customized buffers.

Jan 10, 2025 | bioprocessonline.com | Tyler Menichiello |Crystal Hostler |Mesa Laboratories |Charlie Wakeham

Let Us Handle Your Buffer PreparationThermo Fisher Scientific is here to support you with the buffer preparation in your manufacturing workflow. Leaving the non-core activities to us enables you to focus on the patient therapy development. Our capabilities cover off-the-shelf products like WFI, NaOH, NaCl, or EtOH, a library of the most frequently used buffers that are made-to-order, as well as fully customized buffers.

Sep 19, 2024 | bioprocessonline.com | Mike Ulman |Crystal Hostler |Mesa Laboratories |Robert Ossig

PAT: Build Quality into Biopharmaceutical Processes with Real-Time Monitoring and ControlAutomated aseptic sampling is a process analytical technology (PAT) tool that offers significant benefits for bioprocesses, including reduced contamination risk, higher measurement frequency, and improved efficiency compared to standard manual sampling. As a result, it enables improved process understanding and tighter process control. Learn more here.

Jun 13, 2024 | bioprocessonline.com | Tony Paine |Crystal Hostler |Mesa Laboratories

A ballooning clinical-stage ADC development community is putting stress on both manufacturing capacity and antibody engineering and conjugation talent. What does this burgeon mean for ADC manufacturing, process development, and, ultimately, clinical progress? Join Bioprocess Online Live on July 9th as we navigate the complexity of the ADC manufacturing environment. From linkers to payloads to conjugation, we’ll cover the lay of the land for developers.

Aug 1, 2023 | meddeviceonline.com | Muna Kebede |Matthias Fink |Crystal Hostler |Mesa Laboratories

By Muna Kebede and Matthias Fink, AKRA Team GmbH The EU's Medical Device Regulation, which entered into force in 2021, introduced new requirements for clinical and post-market data for medical devices in Europe. As an additional level of scrutiny for specific devices, the Clinical Evaluation Consultation Procedure ensures that notified bodies correctly assess the clinical data. Let's look at what we can learn from the expert panel's first published scientific opinions.