Here's the recent articles submitted by adam fleming
Articles By adam fleming
Quality Is Not An Organization
Submitted as: Susanne Manz
What does Quality mean to you? Is it a noun meaning an attribute or characteristic measured against a standard or customer requirement? Is it a state of product being free from defects? Is it an organization within your company that is responsible for creating inspection standards or a quality system? Or is it something more? It can be something more powerful for your company.(read
entire article)
View : 251 Times
Category : Others
Death By Capa - Does Your Capa Program Need A Capa?
Submitted as: Susanne Manz
In this webinar, the speaker will discuss the fundamentals of a CAPA program. You will learn how you can make your CAPA program more efficient and more effective.(read
entire article)
View : 223 Times
Category : Business
Save Your Food Business!! - Business Continuity & Disaster Recovery
Submitted as: Angela Bazigos
By attending this webinar you will Understand the important aspects of business continuity, Also will discuss the different types of Disasters, The course will also outline ways to prevent such impact in the future.(read
entire article)
View : 287 Times
Category : Business
Eu Medical Device Regulation (mdr) - Updated Ce Marking Process & Iso 13485:2016 Expectations
Submitted as: Compliance4all
This EU Medical Device Regulation (MDR) 90-minute webinar will discuss the recently developed regulation and its impact on the future compliance and registration of medical devices in the EU.(read
entire article)
View : 345 Times
Category : Others
Process Capability Analysis By Means Of Confidence Reliability Calculations
Submitted as: Compliance4all
The webinar begins with a discussion of relevant regulatory requirements, as motivation for calculating "confidence/reliability". Then, some vocabulary and basic concepts are discussed.(read
entire article)
View : 203 Times
Category : General
Risk Management - Implementing Iso14971: 2019
Submitted as: Compliance4all
In this webinar, the speaker will explain the basic principles and practices of Risk Management approach and Risk Analysis. You will also get an understanding of some of the common errors you may encounter while dealing with risk management.(read
entire article)
View : 199 Times
Category : General
Software As A Medical Device (samd) New Ivdr Document Requirements
Submitted as: Compliance4all
This course will ensure that IVD Diagnostic companies will know exactly what documentation needs to be prepared for a 510(k) regulatory filing, specifically for the software portion of the submittal so that it will be in compliance preventing delays of the 510(k).(read
entire article)
View : 215 Times
Category : Business
European Union Device Regulation (eu Mdr)
Submitted as: Netzealous LLC,DBA -Compliance4all
The EU MDR replaces the MDD and expands the requirements for conformance. The MDR contains 174 pages with 123 "Articles" in 10 "Chapters" and 17 "Annexes".(read
entire article)
View : 210 Times
Category : Business
Drug Master Files: Understanding And Meeting Your Regulatory And Processing Responsibilities
Submitted as: Netzealous LLC,DBA -Compliance4all
This combined Quality Agreement and DMF (Drug Master Files) training will discuss the advantages for suppliers and drug product manufacturers developing these arrangements together.(read
entire article)
View : 214 Times
Category : Business
Controlled Document System For A Life Sciences Manufacturing Plant - Principles Of Lean Documents An
Submitted as: Netzealous LLC,DBA -Compliance4all
All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records.(read
entire article)
View : 214 Times
Category : Business
