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ETQ Releases Reliance NXG QMS and New Quality Events Application
Google Docs collaboration, more efficient management of quality deviations
Qualio Focuses on Building a New, Collaborative Life Sciences Ecosystem
Delivers time, cost, and efficiency savings while streamlining compliance activity
Exemplar Global and QLBS Partner to Launch Audit Simulator
First trial module of learning tool focuses on ISO 9001 and is available now
Greenlight Guru Launches Greenlight Guru Academy
Free education source for global medical device community
Study Finds Quality Shifting From Operational Compliance to Strategic Business Driver
Good quality is adding an average of 11 percent to organizations’ revenue growth
Greenlight Guru Updates Risk Management to Align With ISO 14971:2019
Further enhances change management capabilities
Greenlight Guru Announces New Integration With Jira Software
Creates adaptive system for managing product development and post-market quality for devices with software elements
FDA Opens Voluntary Qualified Importer Program (VQIP) Application Portal
VQIP allows for expedited review and importation for approved applicants that demonstrate safe supply chains
IVT’s Validation Week 2018
An invite from Alcon Laboratories
FDA Plans to Use ISO 13485 for Medical Devices Regulation
Intended to harmonize domestic and international requirements
Pharma Companies Expect Role of Quality Management Teams to Evolve in 2018
Pharma quality teams will have performance-oriented objectives as well as regulatory compliance goals
Hands-On Workshops at IVT’s Quality Risk Management and Change Control 2018
Feb. 27–March 1, 2018, in San Diego
ETQ Announces Acquisition by TCV
Strategic investment positions EtQ to accelerate innovation efforts and growth strategy
This Is Not a Test
The FDA’s RMAT designation goes live
FDA Provides $21.8 Million to States for FSMA Produce Safety Rule Implementation
Awards help states implement multiyear produce-safety systems
Piloting an Improved Intercenter Consult Process
The future of medical product development?
FDA Requests Feedback on Food Labeling Terminology
What does ‘natural’ mean?
AssurX Releases Audit Management Software Update
Manage risk while meeting regulatory requirements and compliance
openFDA Makes Medical Device-Related Data Easier to Access and Use
FDA believes you can use openFDA to create products that promote public health
FDA Pilot Program Encourages Quarterly Malfunction Summary Filings

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