IMMUNO-ONCOLOGY AND THE TUMOR MICROENVIRONMENT

August 20, 2018

The development of cutting edge cancer treatment that uses the immune system is hinged on a better understanding of the tumor microenvironment (TME). The TME provides valuable context for understanding what subtypes of immune cells are present and how to exploit their position and ultimately destroy the tumor cells. Immuno-oncologists are at the forefront of cancer treatment, but the field is evolving fast, and so it is imperative to stay sharp with the latest visualization and analysis techniques.

Spotlight

RASA Life Science Informatics

RASA is a CRO offering solutions and services in the area of Life sciences. With our combined experience in Bio-informatics and Chemo-informatics and strong advisory board, RASA is set to provide premium services in technology solutions, product development and training. We provide our customers with a seamless model of our wide expertise and comprehensive platforms.

OTHER WHITEPAPERS
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The EU Clinical Trials Regulation − What You Need to Know

whitePaper | March 22, 2022

The Clinical Trials Regulation has retained some definitions and refined others. For example the definition of “clinical study”: “Any investigation in relation to humans intended: (a) to discover or verify the clinical, pharmacological or other pharmacodynamic.

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Enabling the Future of Cell & Gene Therapies through Non Proprietary Patient-Owned Data Collection

whitePaper | March 16, 2021

Cell and gene therapies have emerged as a new treatment paradigm, and with them has come the potential to alter the course of many rare diseases. In many cases, there is an opportunity to correct the underlying dysfunction with a one-time administration of a therapy and provide either a functional cure or a substantial improvement in health outcomes. In other cases, long term symptom relief will be the primary therapeutic objective. Some of these indications may require more than one dose to achieve continued symptom relief and scientists and companies are working on technologies that will enable the use of a repeat dose.

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Early engagement and regulatory considerationsfor biotech

whitePaper | May 10, 2022

Biotechnology companies are at the epicenter of innovative drug development, with discoveries spanning from small molecules, large molecules, and biologics to genomic medicines

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Automated Extraction of High Molecular Weight DNA

whitePaper | November 14, 2019

SmartExtraction significantly simplifies the entire automated workflow of DNA extraction, setting new standards with regard to efficiency, yield and quality of the DNA.

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Vaccine and Biologics Development in an Emerging Post Pandemic Landscape

whitePaper | September 20, 2022

It is clear within the global health science industry that analytical biosafety testing and advances in developing scientific technologies will play an important role in drug development’s response to the next pandemic.

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A digital ecosystem for Clinical Trails

whitePaper | July 30, 2021

Clinical trials are complex, lengthy, and resource-inefficient. The clinical research industry is responsible for the delivery of medical solutions to society by systematically evaluating their safety and efficacy in humans during so-called clinical trials. As exemplified by the COVID-19 pandemic, a steady and efficient influx of vaccines, therapeutics, and other innovative medical solutions is critical for meeting society’s current and future medical needs. Unfortunately, the industry faces several persistent issues that make clinical trial operations overly complex, lengthy, and resource-inefficient.

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Spotlight

RASA Life Science Informatics

RASA is a CRO offering solutions and services in the area of Life sciences. With our combined experience in Bio-informatics and Chemo-informatics and strong advisory board, RASA is set to provide premium services in technology solutions, product development and training. We provide our customers with a seamless model of our wide expertise and comprehensive platforms.

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