Another First for Sophia Genetics

The certification also means that Sophia Genetics' proven quality assurance methodology can now be leveraged by clinical laboratories to meet their own quality assurance requirements. Using Sophia Genetics' service, clinical laboratories gain access to quality assurance expertise, facilitating both cost-saving and time-efficient filing for ISO 15189 accreditation and compliance with the new CE-IVD Directive. Sophia Genetics will seek to obtain the CE-IVD mark for all of the genetic tests it supports.

Jurgi Camblong, CEO of Sophia Genetics, said: "The barrier to wider adoption of Next Generation Sequencing (NGS) data for the routine genetic testing of patients has historically been the challenge associated with analysing data. At Sophia Genetics we understand the complexity of NGS data and the need to analyse this data to a clinical standard. We have designed solutions to address even the most difficult data analysis problems that existing bioinformatics software programmes are not able to solve, making NGS genetic testing much simpler, faster and easier for our lab customers."

About CE-IVD
The CE-mark (CE-IVD) indicates that an IVD device complies with the European In Vitro Diagnostics Directive (98/79/EC), and that the device may be legally commercialized and distributed in the EU.

About Sophia Genetics
Sophia Genetics has a fundamentally new approach to the development and clinical adoption of Data Driven Medicine, focused on achieving best patient outcomes whilst keeping patients' personal genomic data secure. Its software as a service (SaaS) offering, dropGen, covers the bioinformatic analysis protocol, the validation and quality control process, the presentation of results of genetic tests to clinicians and the protection of patient DNA sequence data through safe storage and banking.