A common concern for multicenter research trials and sample testing is the consistency of test results at different centers largely because of sample instability. There is concern from reviewers about varying levels of sample degradation because various centers may have the sample stored under differing ambient temperatures and they may test the sample immediately after it arrives or after some delay. This can affect the qualitative and quantitative characteristics of the target molecule and comparing between multicenter research trial results becomes difficult.

Peer group size – i.e. how many “like” users submit data into a QC program is a frequently asked question. With access to a centralized, real-time database of data, is the perceived minimum of 20 valid in today’s laboratory? With improvements to testing systems, QC calculations and immediate data review capability, how do you assess your performance vs. the peer group?

Our experts are ready to discuss effective solutions using particle technology to set up and validate your flow cytometer in a clinical setting, and will specifically address the challenges faced with data collection and flow cytometer performance.

A discussion on newly released TraceFinder 1.1 routine quantitation and targeted screening software plus Transcend front end systems to increase sample throughput. The discussion will be followed by an open Q&A session.

Reliable cold storage is critical for the protection of samples in the clinical lab. In addition, there is an increasing demand for greater security measures in terms of sample accessibility. Today, on-board comuting allows the scientist access to more information than ever before. The development of intuitive health monitoring systems, event logs and enhanced levels of user access are giving scientists peace-of-mind.

A discussion of current LCMS offerings in Vitamin D (both 25 and 1,25D) analysis for research use. Discussions will include a brief overview of workflows and latest application developments followed by a Q&A session.

A discussion of how Procalcitonin (PCT) fits into the earlier diagnosis and risk assessment of sepsis.

Spin towards a lean lab with Thermo Scientific general purpose centrifuges, featuring 3 second Auto-Lock rotor exchange, certified ClickSeal biocontainment rotor lids and unmatched capacity up to 196 blood tubes in a compact footprint, maximizing lab space with ultimate flexibility and productivity.

What is the need in the laboratory for immunosuppressant drug testing? What is most important: turnaround time, cost or tech time and training needed for the method used. Information on both LCMS and immunoassay cost and workflow consideration in the laboratory will be discussed. The differences in the results and the challenges to the transplant team in implementing the results will also be discussed.

Peer group size – i.e. how many “like” users submit data into a QC program is a frequently asked question. With access to a centralized, real-time database of data, is the perceived minimum of 20 valid in today’s laboratory? With improvements to testing systems, QC calculations and immediate data review capability, how do you assess your performance vs. the peer group?

Discover the path toward developing highly pure gene samples with faster throughput through the use of magnetic-based particles. See how these particles can help with the automation and rapid separation of your gene based test.

Thermo Scientific LIS is the first health care informatics solution that combines the sample centric functionality of a LIMS (Laboratory Information Management System) with the patient centric functionality inherent in a traditional hospital or clinical LIS - bridging the gap between the two and delivering a complete and streamlined solution. This new kind of informatics solution will support the burgeoning fields of personalized medicine, companion diagnostics and translational medicine as they enable new approaches to diagnosis, drug development, and individualized therapy.

A discussion of different sample prep and LC methods used to quantify proteins of various abundance with LC/MS, including specific examples. The discussion will be followed by an open Q&A session.

What is the need in the laboratory for immunosuppressant drug testing? What is most important: turnaround time, cost or tech time and training needed for the method used. Information on both LCMS and immunoassay cost and workflow consideration in the laboratory will be discussed. The differences in the results and the challenges to the transplant team in implementing the results will also be discussed.

Reliable cold storage is critical for the protection of samples in the clinical lab. In addition, there is an increasing demand for greater security measures in terms of sample accessibility. Today, on-board comuting allows the scientist access to more information than ever before. The development of intuitive health monitoring systems, event logs and enhanced levels of user access are giving scientists peace-of-mind.

A discussion of how Procalcitonin (PCT) fits into the earlier diagnosis and risk assessment of sepsis.

A discussion of current LCMS options for Drugs of Abuse in Forensic Toxicology and Pain Management analysis. Discussions will include both quantitative and qualitative workflows.

Our experts are ready to discuss effective solutions using particle technology to set up and validate your flow cytometer in a clinical setting, and will specifically address the challenges faced with data collection and flow cytometer performance.

What is the need in the laboratory for immunosuppressant drug testing? What is most important: turnaround time, cost or tech time and training needed for the method used. Information on both LCMS and immunoassay cost and workflow consideration in the laboratory will be discussed. The differences in the results and the challenges to the transplant team in implementing the results will also be discussed.

Peer group size – i.e. how many “like” users submit data into a QC program is a frequently asked question. With access to a centralized, real-time database of data, is the perceived minimum of 20 valid in today’s laboratory? With improvements to testing systems, QC calculations and immediate data review capability, how do you assess your performance vs. the peer group?

Learn how to get the quantitative information and better results that clinicians demand when developing new diagnostic tests such as lateral flow. Our solution to improving the value of your current test would be upgrading from colloidal gold to polystyrene particles.

Spin towards a lean lab with Thermo Scientific general purpose centrifuges, featuring 3 second Auto-Lock rotor exchange, certified ClickSeal biocontainment rotor lids and unmatched capacity up to 196 blood tubes in a compact footprint, maximizing lab space with ultimate flexibility and productivity.

A discussion on newly released TraceFinder 1.1 routine quantitation and targeted screening software plus Transcend front end systems to increase sample throughput. The discussion will be followed by an open Q&A session.