Cleaning Validations Using Extraction Techniques by Compliance Global Inc.
Cleaning validation guidelines are an essential step in the medical device development. One of the most common methods is using extraction techniques to validate the cleanliness of a device. This webinar will provide valuable guidance on how to achieve a thorough validation of a cleaning process.
New Hyde Park, NY, September 24, 2015 --(PR.com)-- Overview: Cleaning validation guidelines are an essential step in the medical device development. One of the most common methods is using extraction techniques to validate the cleanliness of a device. This webinar will provide valuable guidance on how to achieve a thorough validation of a cleaning process.
Why Should You Attend:
Medical device manufacturers have always been under scrutiny to ensure that their product does no harm for healthcare services. Regulatory agencies have become increasingly aware of the potential dangers of residual materials on medical devices. Therefore, cleanliness has become a hot topic in the medical device community.
The March 2015 publication of the FDA Guidance for “Reprocessing Medical Devices in Health Care Settings” has made the FDA validation stance very clear: cleaning processes must be validated. A thorough validation of the cleaning processes used to remove residual materials from both newly manufactured and reprocessed medical devices is necessary to ensure patient safety.
Areas Covered in this Webinar:
Cleaning Validation Overview
Defining the Scope
Identifying the Contaminants
Choosing the Test Method
Choosing the Solvents
Setting Extraction Parameters
Validating the Extraction
Setting Limits
Learning Objectives:
How to validate a cleaning process
What testing is appropriate for a cleaning validation
How to validate the extraction technique
Who Will Benefit:
QA/QC Managers
QA/QC Personnel
Validation Managers
Validation Personnel
Medical Device Manufactures
Level:
Beginner
For more information, please visit bit.ly/1fAYmR3
About Compliance Global Inc:
Compliance Global Inc; is a training (webinar) organization based in New Hyde Park, New York, providing world-class compliance trainings and online webinars by leveraging a pool of experienced speakers / consultants in the Pharmaceutical, Bio-Technology, Medical Devices, Clinical Compliance, FDA Compliance, Healthcare, BFSI, Life Science & HR streams for improving the knowledge base of the customers. Our trainings are contemporary, simple and cost-effective with easy access and great delivery experience. Compliance Global is a multifaceted entity, an absolute knowledge repository.
Our varied industry expertise ranges across Life Science (Pharmaceutical, Bio-Technology, Medical Devices, Clinical Compliance, FDA Compliance), Healthcare, HR Compliance, BFSI, Food & Dietary Supplements, Insurance, Accounting & Taxation and other Cross Industry streams.
Email: referrals@complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
Why Should You Attend:
Medical device manufacturers have always been under scrutiny to ensure that their product does no harm for healthcare services. Regulatory agencies have become increasingly aware of the potential dangers of residual materials on medical devices. Therefore, cleanliness has become a hot topic in the medical device community.
The March 2015 publication of the FDA Guidance for “Reprocessing Medical Devices in Health Care Settings” has made the FDA validation stance very clear: cleaning processes must be validated. A thorough validation of the cleaning processes used to remove residual materials from both newly manufactured and reprocessed medical devices is necessary to ensure patient safety.
Areas Covered in this Webinar:
Cleaning Validation Overview
Defining the Scope
Identifying the Contaminants
Choosing the Test Method
Choosing the Solvents
Setting Extraction Parameters
Validating the Extraction
Setting Limits
Learning Objectives:
How to validate a cleaning process
What testing is appropriate for a cleaning validation
How to validate the extraction technique
Who Will Benefit:
QA/QC Managers
QA/QC Personnel
Validation Managers
Validation Personnel
Medical Device Manufactures
Level:
Beginner
For more information, please visit bit.ly/1fAYmR3
About Compliance Global Inc:
Compliance Global Inc; is a training (webinar) organization based in New Hyde Park, New York, providing world-class compliance trainings and online webinars by leveraging a pool of experienced speakers / consultants in the Pharmaceutical, Bio-Technology, Medical Devices, Clinical Compliance, FDA Compliance, Healthcare, BFSI, Life Science & HR streams for improving the knowledge base of the customers. Our trainings are contemporary, simple and cost-effective with easy access and great delivery experience. Compliance Global is a multifaceted entity, an absolute knowledge repository.
Our varied industry expertise ranges across Life Science (Pharmaceutical, Bio-Technology, Medical Devices, Clinical Compliance, FDA Compliance), Healthcare, HR Compliance, BFSI, Food & Dietary Supplements, Insurance, Accounting & Taxation and other Cross Industry streams.
Email: referrals@complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
Contact
Compliance Global Inc
Roger Davis
+1-516-900-5515
http://bit.ly/1fAYmR3
Email: support@complianceglobal.us
Toll Free: +1-844-746-4244
Fax: +1-516-900-5510
Roger Davis
+1-516-900-5515
http://bit.ly/1fAYmR3
Email: support@complianceglobal.us
Toll Free: +1-844-746-4244
Fax: +1-516-900-5510
Contact
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