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Supporting Life Sciences at every stage

Developments in the enabling science and technologies have lead to a data explosion in the life sciences sector Genomics is the study of the structure and function of genes, by mapping, sequencing and analysing genomes (full DNA sequences). Proteomics is the study of the protein complement (proteome) generated from a genome, including the structure, function and interactions of the proteome. Over the years, developments in the enabling sciences and technologies used by the life sciences sector has led to an exponential increase in the amount of data that is managed, processed and analyzed. Tessella's expertise and experience covers all these disciplines.

We are one of the UK's leading independent suppliers of software solutions to the pharmaceutical, agrochemical, biotech and medical communities, with a growing presence in the European and US markets. We pride ourselves in establishing long-term relationships with our customers. Over two decades of experience working with major pharmaceutical and agrochemical companies, and businesses involved in emergent technologies such as bioinformatics and pharmacogenomics, means we can understand your business requirements and work with you to provide innovative, cost-effective solutions, throughout your discovery, development, testing and registration pipeline. Our expertise and skills can also be applied to emerging technologies such as PAT.

Tessella understand your business requirements and can provide innovative, cost-effective solutions throughout the whole drug pipeline Since 1998, Tessella has been helping to drive innovation in drug development by enabling the deployment of Adaptive Clinical Trials. Tessella has implemented statistical models for phase 1 trials, phase 2 dose finding studies using Bayesian statistics, and phase 2/3 seamless designs. Tessella has supported these models by developing simulation and analysis tools, and by building and running the infrastructure to run the trials. Such infrastructure has included central randomization, electronic data capture, and drug supply management. Tessella has also worked with pharmaceutical companies to enhance their own in-house systems so that they can support Adaptive Clinical Trials.

We also offer decision analysis & portfolio management and PK/PD modelling.

Tessella's certified Quality Management System, established in 1992, ensures that quality is built into our software development process. This allows us to excel in providing you with FDA Rule 21 CFR Part 11 compliance, and means we understand the issues involved in GLP, GMP and GCP.

One of Tessella's many strengths is our ability to extract relevant technologies from projects in other sectors, and apply them in novel ways in life sciences. One of Tessella's many strengths is our ability to extract relevant technologies from projects in other sectors, and apply them in novel ways in life sciences. All these skills can be employed when we work with you to help maintain your competitive advantage.

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Tessella Experience Capability Statement  Tessella - Supporting Life Sciences at every stage
Strategic Planning Capability Statement  Decision Analysis, Portfolio Management and Roadmap Development
Capability Statement  Portfolio Management Offerings
Technical Article  Critical decisions - an objective approach (Tessellations Edition 62, page 2)
Case Study  Portfolio Management at UCB
Adaptive Clinical Trials News  Adaptive Clinical Trials in the media
Capability Statement  Adaptive Clinical Trials – Offerings and Experience
Capability Statement  Adaptive Clinical Trials Simulation Toolkit
Capability Statement  Exploiting Seamless Adaptive Clinical Trials and Seamless Adaptive Clinical Trials: The Maths
Capability Statement  Bayesian Statistics in Clinical Trials
Technical Article   Adaptive Clinical Trials – Working at the cutting-edge (Tessellations Edition 57, page 1)
Case Study  Software for cancer clinical trial
Case Study  Development of clinical trials database for products and services company
Case Study  System for palmtop collection of clinical trials data
Bioinformatics Case Study  Bioinformatics mining database for leading biotech
Genomics Case Study  Development of human genetics web application for Wellcome Trust Centre
Proteomics Case Study  Mass spectrometry data analysis pipeline for leading biotech
Case Study  2D electrophoresis gel matching
Case Study  Analysis and visualization of electrophoresis gel data
Data Acquisition Case Study  Electrophysiology automation system for GSK
Case Study  Aptamer assay template development for Archemix
Technical Article  Electronic Data Capture
Data Management News  Consultancy on information management of genetic testing system for Wessex Regional Genetics Laboratory
Case Study  Mass spectrometry repository for leading biotech
Case Study  Automated management system for compound library for The Automation Partnership
Digital Preservation Technical Article  Digital Archiving in the Pharmaceutical Industry
Capability Statement  Digital Archiving Offerings
Technical Article  Archiving Electronic Information
Case Study  Central electronic archive for major pharmaceutical company
Data Analysis and Visualization Capability Statement  Bayesian Statistics in Health Diagnostics
Technical Article  Developing Excel Addins
Technical Article  Computer Image Processing
Case Study  Spectrum visualization tool for AstraZeneca
Case Study  Data analysis and visualization tool for a leading biotechnology company
High Throughput Technologies News  THERM™– Managing and measuring higher experimental throughput
Technical Article  High Throughput Screening
Capability Statement  High Throughput Experimentation and Tessella
Case Study  Development of ultra-HTS system for The Automation Partnership
Case Study  The use of HTE to allow researchers to innovate at a world-leading consumer products company
Case Study  Automated Salts and Polymorph screening for GSK
Process Automation and Control Capability Statement  Robotics and Laboratory Automation
Capability Statement  Workflow: automating business processes
Technical Article  Workflow systems
Case Study  System for screening and testing of chemical production techniques for GSK
LIMS and Sample Tracking Technical Article  Beyond LIMS: the integrated data pipeline (Tessellations Edition 52, page 3)
Technical Article  Beyond LIMS: the integrated data pipeline
Technical Article  Electronic Laboratory Notebooks
Technical Article  Choosing and using a LIMS
Technical Article  Maintaining quality with Robotics and LIMS
Technical Article  Integrated Laboratory systems
Case Study  LIMS upgrade and migration for major LIMS producer
Case Study  Development of micro-array LIMS for Medical Research Council
Case Study  LIMS consultancy for leading biotech
Case Study  A Mass Spectrometry analysis pipeline
Case Study  Integrated data pipeline for Oxagen
510(k) and V&V Activities Capability Statement  Software for regulated industries
Case Study  FDA 510(k) compliant software development and testing for medical device manufacturer
Case Study  FDA compliant software development for Remote Diagnostic Technologies Ltd
FDA Compliance Technical Article  Process Analytical Technology (Tessellations Edition 54, page 1)
Technical Article  21 CFR part 11 compliance
Technical Article  21 CFR part 11 compliance – developments

For reasons of commercial confidentiality, we are not able to reveal details of a significant proportion of our projects.

 

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Last Updated: 30-Apr-2008