|
Medical Devices: Handling, Storage, Distribution, and Installation
Tuesday
01.00 PM
http://c2gowebinars.com/product/?topic=medical-devices-handling-storage-distribution-and-installatio
10777 Westheimer Suite 1100, Houston, Texas, USA,
Houston Texas 77042
Report Abuse
|
|
DESCRIPTION
Handling, Storage, Distribution, and Installation procedures need to be established for all manufacturers of medical devices. These procedures define and control how devices are handled, stored, distributed, and installed with customers. The objectives of these regulations are to ensure the quality of in-process and finished devices is not compromised and to ensure there are no product mix-ups, damage, deterioration, or contamination.
The processes and controls for release of product through the various stages within production, into finished inventory, through market distribution all need to be defined, with clear control points which prevent release and use of product which has not completed all required manufacturing and test stages.
Distribution records should be maintained which record what devices were shipped, when they were shipped, and where they were shipped to and also record any necessary identification and traceability identifiers.
If there are environmental requirements for the device in storage and in transit, then these need to be defined and controls established to ensure such environmental requirements are continually achieved.
Where a device has specific installation requirements, the requirements need to be documented and processes established and monitored to ensure correct installation.
Why you should attend:
Handling, Storage, Distribution, and Installation are often forgotten and neglected parts of the Quality Management System (QMS) for medical device companies. But, failure to fully establish these processes in your company can still have a serious impact on your company and on your customers. Failures can negatively impact your business in terms of manufacturing efficiencies, inventory levels, scrap, yields, and more. Even more importantly, failures can lead to customer delays, dis-satisfaction, complaints, quality problems, recalls, and more. This webinar will help you avoid these costly and painful problems.
Areas covered in the Webinar:
This webinar will cover:
Handling processes
Preventing Mix-ups, damage, deterioration, contamination
Storage requirements including stock rotation
Environmental controls
Authorizing receipt and dispatch from storage areas
When a product?s fitness for use / quality deteriorate over time
Identification of products
Installation procedures including inspection and testing
Important linkages to other QMS requirements
Who will benefit:
QMS Auditors
Quality Engineers
Manufacturing Engineers
Field Service and installation engineers
Manufacturing Supervisors
Manufacturing/ Production /Operations/ Distribution Supervisors, Managers, and Directors
Plant Managers
Quality Managers
Employees new to Medical Device Companies
Webinar includes:
Q/A Session with the Expert to ask your question
PDF print only copy of PowerPoint slides
90 Minutes Live Presentation
Certificate of attendance
For?Registration?:??http://c2gowebinars.com/product/?topic=medical-devices-handling-storage-distribution-and-installation
Note:?Use?coupon?code????and?get?15% off?on?registration.
|
compliance2go
Phone: 8777824696
Fax: 8777824696
Email: subscribe (at) compliance2go.com |
|
|
| Report Abuse |
|
|
| |
| |
|
| List your Event |
| | Similar Events | Houston: Introduction to Risk Management: Medical Devices
DESCRIPTION
This webinar will cover Risk Management per ISO 14971 throughout the product lifecycle. Risk Management is an important process to methodically and effectively identifying and mitigating risks in the product design and manufacturing p
Date Posted: 18-Apr-16
| Houston: CAPA for Medical Device Companies
DESCRIPTION
This webinar will help you ensure an efficient and effective CAPA process leading to improved quality and compliance for your company. You?ll learn how to streamline and monitor your process to ensure compliance and improved performan
Date Posted: 18-Feb-16
| FL: Live Webinar Use / Human Factors Engineering to Satisfy the New IEC 62
Live Webinar Use / Human Factors Engineering to Satisfy the New IEC 62366-1, -2
Description
IEC has released a new medical device usability standard, IEC 62366-1:2015 -- Part 1: “Application of the new Usability Engineering Standard to Medic
Date Posted: 30-Apr-18
| FL: Live Webinar Understanding and Applying the New EU Medical Device Regu
Live Webinar Understanding and Applying the New EU Medical Device Regulations (EMDR)
Description
The European Parliament just adopted the Medical Devices (MDR) and In vitro Diagnostic Medical Devices (IVDR) regulations. The adoption
Date Posted: 26-Apr-18
| Houston: Auditing the Risk Management File - By Dan O Leary
DESCRIPTION
Medical device manufacturers must implement risk management systems for their devices. This can be a complicated system requiring a lot of work and multiple resources. If it is not correct, the regulatory authorities may require correc
Date Posted: 02-Feb-16
| FL: Live Webinar FDA’s Final Rule Regarding Device Establishment Registrat
Live Webinar FDA’s Final Rule Regarding Device Establishment Registration and Listing: Procedure on How to Register and List
Description
Device firms, establishments or facilities that are involved in the production and distribution of me
Date Posted: 27-Apr-18
| Houston: Medical Devices - ISO 13485 ? Do you really know what you need to?
DESCRIPTION
A detailed look at each section of the standard.
Real world examples of what to expect, and what to prepare and repeal within the audit guidelines.
What must a documentation system look and feel like to ensure compliance?
These and
Date Posted: 18-Apr-16
| FL: Live Webinar FDA’s Final Rule Regarding Device Establishment Registrat
Live Webinar FDA’s Final Rule Regarding Device Establishment Registration and Listing: Procedure on How to Register and List
Description
Device firms, establishments or facilities that are involved in the production and distribution of medica
Date Posted: 08-May-18
| Houston: Internal Audit is a Secret to Medical Device Compliance
DESCRIPTION
Internal Audit is an incredibly powerful tool to identify areas of non-compliance. A well designed audit program is a critical tool in understanding, communicating, and mitigating compliance risk. This webinar will help companies use
Date Posted: 18-Feb-16
| Boston: 2 DAY SEMINAR Effective Compliance Strategies for Complaint Handling,
2 DAY SEMINAR Effective Compliance Strategies for Complaint Handling, Medical Device
Location 1: Boston,MA
Jul 11 - 12
Description
Complaint handling systems have come under intense scrutiny by the FDA in recent years and enforcement trends
Date Posted: 04-May-18
| Houston: Due Diligence ? Quality and Compliance Aspects for Medical Device
DESCRIPTION
Mergers and acquisitions are an on-going and important part of the medical device industry. And Due Diligence is a critical part of that process, setting the stage for either success or disaster. Poor due diligence can lead to qual
Date Posted: 18-Apr-16
| FL: Live Webinar Design Control Under 21 CFR 820 (the CGMPs) and ISO 13485
Live Webinar Design Control Under 21 CFR 820 (the CGMPs) and ISO 13485
Description
The FDA CGMPs (21 CFR 820.30) and ISO QMS’ (ISO 13485:2016 7.3) expect companies to perform meaningful, results driven Design Control act
Date Posted: 27-Apr-18
| FL: Live Webinar Corrective and Preventive Action (CAPA) - Principles of L
Live Webinar Corrective and Preventive Action (CAPA) - Principles of Lean Documents and Lean Configuration
Description
Design controls involve the translation of user requirements (aka Voice of the Customer) into specific technical requirements a
Date Posted: 08-May-18
| Houston: Mobile Devices and HIPAA ? Managing Risks and Improving Productivity
DESCRIPTION
This session will review the requirements and current issues pertaining to mobile devices and present ways for the attendees to consider how to meet patient desires and stay within the regulations, including processes for managing port
Date Posted: 18-Apr-16
| FL: Live Webinar Construct and Manage the Technical File and Design Dossie
Live Webinar Construct and Manage the Technical File and Design Dossier
Description
This Webinar will provide a substantive overview and outline differences between the Technical File and Design Dossier for those device firms dealing with the glo
Date Posted: 30-Apr-18
|
|
Map locations are shown as per geocoding services and they depeneds on the accuracy of the address. If address is wrong it may show wrong map. If you put a listing which shows wrong map, please remove the listing and create a new one with correct address details.
Please note: The information on this site is submitted by users. CanadianDesi never checks accuracy of the information. Please use this information at your risk. If you have any question or concern regarding this listing, or you know that the above information is not accurate, please Contact Us. Thanks.
|
| Please note: The information on this site is submitted by users. CanadianDesi never checks accuracy of the information. Please use this information at your risk. If you have any question or concern regarding this listing, or you know that the above information is not accurate, please Contact Us. Thanks.
|
|
