Webinar On Medical Devices Designing with Cleanliness in Mind

Compliance Trainings, Canada
2015-02-09

Description :

Cleanliness is a hot topic in the medical device industry. The FDA expects medical device companies to validate the cleanliness of their devices. One of the best ways to achieve a clean device is by designing it with cleanliness in mind.

This 60 minutes webinar will provide in-depth and valuable guidance to medical device manufacturers on design considerations for both single-use and re-usable devices. There are certain design elements that are more difficult to clean and should be avoided whenever possible. With the "right" design, both the manufacturing and cleaning processes can be simplified.

Areas Covered in the Session :

Design Requirements

Single-Use Design Considerations

Re-usable Design Considerations

Design Elements to Avoid/Minimize

Simplifying the Manufacturing Process

Simplifying the Cleaning Process

Who Will Benefit:

QA/QC managers and personnel

Validation managers and personnel

R&D and Engineering

Manufacturers of Implantable Medical Devices

Manufacturers of Single-Use Medical Devices

Manufacturers of Reprocessed/Reusable Medical Devices

Price Tags:

Live

Single Live : For One Participant

$ 249

Corporate Live : For Max. 10 Participants

$ 899

Recording

Single REC : For One Participant - Unlimited Access for 6 Months

$ 299

For more information and enquiries contact us at

Compliance Trainings

5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : 4169154458 
Email : support@compliancetrainings.com

Speaker Profile

Kierstan Andrascik, founder of QVET Consulting, with her years of experience in the medical device industry assists manufacturers with their validation needs. She specializes in cleaning validations for both new and reprocessed medical devices and has established herself as one of the foremost experts in medical device cleanliness. She also provides guidance in many other areas including sterilization, biocompatibility, packaging, and materials characterization. Previously, she worked at Nelson Laboratories in Salt Lake City, Utah where she served as study director covering a variety of testing including new device cleaning validations, materials characterization, and package testing.

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