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Global medical device manufacturer will present a case study at the IVT validation week Europe conference on the Efficient Paperless Validation approach through ValGenesis VLMS

Fremont, CA, March 29, 2017– ValGenesis, Inc., the world’s leading provider of Validation Lifecycle Management System (VLMS) software solutions, today announced that a globally renowned Medical Device manufacturer will be presenting a case study about their experience with the paperless validation process. In the study, the medical device manufacturer explains how the paperless validation process helped to improve upon their...

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World’s leading Medical Technology Company Implements ValGenesis (VLMS) to Augment Revised Validation Management Process Globally

Fremont, CA. June 14, 2016: ValGenesis, a leading provider of paperless validation lifecycle management software solutions, today announced the launch of its successful relationship with the World’s Leading Fortune 500 Medical Technology organization. The leading device company enhances Orthopedics, Medical and Surgical arenas, providing innovative products and services that help patients lead healthier and improved lives. The global leading manufacturer...

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A Global Leading Healthcare Technology Company Implements ValGenesis Cloud Solution for Validation Lifecycle Management

May 30, 2016, Fremont, CA: ValGenesis, Inc., the market leader in Enterprise Validation Lifecycle Management Solutions (VLMS) is pleased to announce that an innovative Netherlands based global healthcare technology company went live with ValGenesis Validation Lifecycle Management System. The healthcare technology company, which offers high quality medical devices, patient monitoring products and accessories in over 100 countries made the choice to...

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ValGenesis Ventures its Validation Lifecycle Management System into the Blood Industry and Collaborates with a Leading Plasma-based Product Company

Fremont, CA. May 17, 2016: ValGenesis opened a new avenue of opportunity with a leading Plasma based product company that has implemented the paperless Validation Lifecycle Management System (VLMS) into their plasma donor collection centers. The Blood Services industry must ensure compliance with several agencies including the Food & Drug Administration, (FDA), the Center for Biologics Evaluation and Research (CBER),...

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ValGenesis Inc. Successfully Completes Service Organization Controls 2 (SOC 2) Report under AT Section 101 for the Second Consecutive Year

FREMONT, CA, May 10, 2016 - ValGenesis Inc., the market leader in enterprise Validation Lifecycle Management Software solutions, announced today that it has completed its Service Organization Controls 2 (SOC 2) examination under AT Section 101, Attest Engagements (AICPA, Professional Standards) for the period of January 1st 2015 through December 31st 2015 for the second consecutive year. The SOC 2 examination is...

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Foremost Global Medical Device Manufacturer Selects ValGenesis Validation Lifecycle Management System to Streamline the Validation Process across Global Manufacturing Sites

April 28, 2016 – ValGenesis, Inc., the market leader in Enterprise Validation Lifecycle Management Solutions (VLMS) today announced that a prominent world provider of products and services for sufferers of chronic kidney failure has selected ValGenesis Validation Lifecycle management System to manage their corporate validation process. The global medical device manufacturer had been seeking a software solution to manage their...

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ValGenesis Inc. Successfully Completes ISO 9001:2008 Surveillance Audit – Completion Demonstrates the Company’s Strong Commitment to Continuous Process Improvement

Fremont, CA – April 21, 2016 – ValGenesis Inc., the market leader in Enterprise Validation Lifecycle Management Solutions (VLMS) today announced thatit had successfully completed the ISO 9001:2008 surveillance audit focused on the development, implementation and maintenance of its software and services. Certification to ISO 9001 requires an accredited third party auditing organization to thoroughly review the company’s internal quality management system...

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ValGenesis Inc. Successfully Completes Service Organization Controls 2 (SOC 2) Report under AT Section 101

FREMONT, Calif., April 1st, 2015 - ValGenesis Inc., the market leader in enterprise Validation Lifecycle Management Software solutions, announced today that it has completed its Service Organization Controls 2 (SOC 2) examination under AT Section 101, Attest Engagements (AICPA, Professional Standards) for the period of January 1st 2014 through December 31st 2014. The SOC 2 examination is performed in accordance with AT...

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Varian Medical Systems Implements ValGenesis Cloud Solution for Validation Lifecycle Management

FREMONT, Calif. – Dec. 8, 2014 – ValGenesis, Inc., the innovator and market leader in Enterprise Validation Lifecycle Management Solutions (VLMS), today announced that Varian Medical Systems, the world’s leading manufacturer of medical devices and software for treating cancer, has implemented the cloud-based ValGenesis system. Varian has successfully gone live with ValGenesis to manage its validation lifecycle processes for enterprise...

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ScinoPharm Selects ValGenesis VLMS 3.0 to Manage Validation Lifecycle Processes

FREMONT, Calif., June 23, 2014 /PRNewswire/ — ValGenesis, Inc., the market leader in Enterprise Validation Lifecycle Management Solutions (VLMS) today announced that ScinoPharm Taiwan Ltd., a manufacturer of potent compound API and finished drug products, has implemented and successfully gone live with the ValGenesis VLMS 3.0 – Validation Lifecycle Management Solution to manage their validation lifecycle processes. ScinoPharm has been...

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Dr. Ajaz Hussain to Serve as an Advisor to ValGenesis, Inc.

FREMONT, Calif., Jan. 21, 2014 /PRNewswire/ — ValGenesis, Inc., the market leader in Enterprise Validation Lifecycle Management Software solutions , today announced that Dr. Ajaz Hussain has agreed to serve as Senior Technical and Regulatory Advisor to ValGenesis. Regulated Life Sciences companies are required to plan, implement and document validation activities for every aspect of drug manufacturing and quality assurance....

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