OASIS solution for GE Ultrasound multi site production
GE Ultrasound success story on the implementation of Orcanos and Polaris joined technology solution for production floor real time reporting and analysis tool.
View Article10 Tips on How To Keep Your Good Manufacturing Practice and Making GMP At Top
Everyone involved in the manufacturing and processing of FDA regulated products, has the responsibility to do their best to ensure that every product we manufacture is safe, pure and of the highest...
View ArticleOrcanos QPack™ ALM Software CUSTOMER SUCCESS STORY of AB Dental
AB Dental’s recent growth required upgrading of the Quality Management System, in order to address the different regions of the company. After several audits, the company decided to strengthen the...
View ArticleTip of the Week – Use QPack Change Management Tools To Review Your Documents
October 7nd 2015 Rami Azulay in Tip of the Week, QPack First for those of you who asking why this is important, then I wish to recall what we do today when we are using Office tools. When we use...
View ArticleClosed System LOOP FDA Recommended CAPA Methodology
In this paper we are going to examine the quality of the event management process, and in particular the CAPA, referred to as corrective and preventive action. As we think about the quality management...
View ArticleHo to do change management in QPack
October 13 2015 Zohar Peretz in Tip of the Week, QPack This is our recommended change management process in a nutshell Use a specific work item for change request (usually its the CR work item)...
View ArticleTip Of The Week – Build yourself an Aggregative QPack Solution for Cross...
October 7th, 2015 Avi Harrary in Tip of the Week, QPack Start Your Free Trial Now This week’s tip addresses how we deal with complex technology such as medical devices, smart phones, or any...
View ArticleTip Of The Week – Use QPack ALERTS To Keeps People On The Same Page
October 25th 2015 Amita Gupta in Tip of the Week, QPack Start Your Free Trial Now Use QPack ALERTS To Keeps People On The Same Page Alerts are very powerful tools useful in keeping track of...
View ArticleTip Of The Week – How to Build Your Design Inputs/Outputs in QPack According...
October 25th 2015 Rami Azulay in Tip of the Week, QPack Start Your Free Trial Now Post Overview If you are a medical device vendor, then you are probably aware of how the ISO 13485 methods of...
View ArticleHow to Build Smart KPI View To Measure Your R&D Performance
December 31, 2015 | Rami Azulay | in Tip of the Week, QPack Post Overview Whether you are a medical device vendor or non-regulated SVP, most of your resources should be spent on your research and...
View ArticleTip Of The Week – Why ORCANOS | ALM and GitHub Can Work So Good Togther
The Branch Concept – Powerful Tool To Control Your Product Lifecycle and Not Just Your Code April 11th, 2016 Rami Azulay in Tip of the Week, QPack This week’s tip expounds on the GitHub concept of...
View ArticleEffective baseline management for ORCANOS | ALM Test Management
By Rami Azulay on June 29, 2016 Test Management, ORCANOS | ALM ORCANOS | ALM versions and baseline management has similar behavior as a source control, thus provides powerful and intuitive tools to...
View ArticleOrcanos announce QMR as a local partner in the United States
At Orcanos Software, we are proud to announce that QMR have become a certified partner, as part of our Alliance Partnership program. This partnership will allow Orcanos to improve the quality of...
View ArticleWhat is the Traceability Data Model for Medical Device Development?
By Rami Azulay on June 20, 2016 ALM Management, ORCANOS | ALM Good Development Practices (GDPs) can be defined as the requirement to describe facilities and equipment; to document established...
View ArticleHow to Team Up an Effective/High Performance Test Organization with Strong...
There are three key terms in the title of this article. The first is team, the second is high performance, and the third is lead. We are going to be talking about each one of these terms. Whenever I...
View ArticleTip Of The Week – What is Significant Software Change in Medical Device?
Changes to Software Many changes to a device’s software will require a licence amendment application. As software developer you may need to answer some criteria by the QA. The following may help you...
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