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SelectScience® je inovativní online vydavatel v oboru vědy, který propojuje vědce s informacemi a pomáhá jim při výběru nejlepší laboratoře prostřednictvím kombinace bohatého obsahu, informací typu peer-to-peer a důvěryhodných recenzí produktů
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Future‑ready biobanking starts with smarter sample storage

Pá, 26.6.2026 16:00 CEST
Chraňte integritu vzorků v biobankách a klinickém výzkumu. Zjistěte, jak od expertů z Thermo Fisher Scientific optimalizovat skladování, sledovatelnost a soulad s předpisy.
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Select Science: Future‑ready biobanking starts with smarter sample storage
Select Science: Future‑ready biobanking starts with smarter sample storage

Biobanking and clinical sample storage sit at the heart of modern research, where the value of every specimen depends on its integrity, traceability, and long‑term stability. As sample volumes grow and regulatory expectations tighten, laboratories face a relentless demand for robust identification systems, streamlined workflows, and reliable storage practices that safeguard data quality across the entire lifecycle of a sample.

Join this SelectScience® webinar for expert advice on the best practices in sample storage identification, with a focus on maintaining sample integrity, reducing risk, and ensuring compliance in regulated environments. Hear directly from two Thermo Fisher Scientific experts, Dr. Dolly Casper and Amy Armstrong, as they share innovative solutions designed to enhance reliability, traceability, and operational efficiency in biobanking and clinical settings.

Attend this webinar and gain insight into how to optimize end-to-end workflows across collection, storage, tracking, and retrieval, while supporting scalability and lab modernization.

Certificate of attendance

If you attend the live webinar, you will automatically receive a certificate of attendance, including a learning outcomes summary, for continuing education purposes.

If you view the on-demand webinar, you can request a certificate of attendance by emailing [email protected].

Webinar details
  • Cost: Free to attend
  • Location: Online
  • Duration: 60 minutes per session

Registration is required to secure your place. If you register but can’t attend live, you will receive a link to the on‑demand recording once it becomes available

Who should attend?

This event is perfect for:

  • Biobank mangers and directors
  • Lab managers
  • Operations managers
  • Biopharmaceutical contract research organizations (CROs)
  • CRO operation leads
  • Clinical trial leads
  • Professionals in biopharmaceuticals
  • Academics
  • Professionals in biotechnology
What will this webinar cover?
  • How to protect sample integrity and reduce risk across the sample lifecycle
  • Best practices for compliant and reproducible sample storage and identification
  • Integrated workflows from collection to analysis for improved efficiency
  • Strategies to scale biobanking operations and modernize laboratory processes

Speaker: Dr. Dolly Casper (Product Manager, Thermo Fisher Scientific)

Dr. Dolly Casper is the Product Manager for the Manual Cryopreservation Storage Portfolio. She has 11 years of experience driving reliable sample preservation and workflow optimization. Dr. Casper holds a PhD in Bioengineering and completed a postdoctoral fellowship in tissue engineering, with expertise in cell culture applications.  

Speaker: Amy Armstrong (Senior Product Manager, Thermo Fisher Scientific)

Amy Armstrong obtained a BS from Michigan State University and MBA from Walsh College. She currently acts as the Senior Product Manager across biobanking and cryopreservation for automation storage product portfolio. She focuses on understanding the biobanking market, customer’s workflow, and sample storage protocol. 

Moderator: Olivia Long (Editorial Team, SelectScience)

Olivia Long is a science editor specializing in pharmaceutical and applied science. She has a BSc in Pharmacology, and an MSc in Neuroscience, where she investigated neuro‑oncology drug‑resistance pathways using patient‑derived cell models. Her laboratory experience spans R&D hygiene testing, controlled‑environment sample production, and protocol development, giving her a broad understanding of analytical workflows and the scientific principles underpinning biopharmaceutical quality control.

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