2014 - Webinar On Medical OEM Design Control Audit: Anticipation and Expectations

This 60 minute webinar on a Design Control Audit by the FDA and other bodies will provide an understanding of what a medical OEM should anticipate during an audit during a design control audit. All medical device companies that are in need of examining their design control process should be aware of what to expect.
The FDA and other authorizing bodies have become more stringent in their examination of medical OEM procedures, process, and data. Many medical industry companies have not completed all their testing and design reviews before commercializing products properly or brought their mature product lines up to current FDA standards and are not in total compliance. This webinar shows the process to be followed for developing a standard procedure to identify what is expected for design control.
For example, companies should be compliant to 21 CFR 820, ISO 13485:2003, ISO 14971:2007, etc. Design History Files and validations need to be up to date to meet current standards. The FDA and other authorizing bodies expect continuous improvement and risk management to be integrated into the company quality system. Old medical devices need to have a risk assessment for each product and updated validations for product and processes. It should describe the risk acceptance criteria as well as roles and responsibilities of each member on the team.
In this webinar, we will discuss practical steps you can follow to make sure your product design control and quality files are ready for an audit. It will also give the attendee guidelines on how to deal with the authorizing bodies.
Areas Covered in the Session :
Champion/Multi-functional team approach/responsibility
Dealing with the FDA and other authorizing bodies
Phase by phase design process check list
Design input/output
Design verification/validation
Design changes
Design review
Design History File (DHF)
Due-diligence
Gap analysis ? data gathering for the design history files
Risk assessment
Design changes
483 warning letters
Planning to be prepared
Who Will Benefit:
This webinar will provide valuable assistance and give a process to all medical device and regulated companies that need to prepare for an FDA or authorizing bodies audit in the future. The employees who will benefit include:
OEM and CMO quality managers
OEM and CMO quality engineers
End-users responsible for design control and technical files
R&D and product development
Process engineers and managers
Operations and plant management
Validation engineers
Remediation teams
QA, Regulatory Affairs
QC and Corporate Auditors
All team members who contribute to design history files, clinical, verifications/validations, risk management or technical files
Consultants
Project managers
Supplier management
Product transfer engineers
All Contract Manufacturers working in the medical industry
Speaker Profile
Robert Braido has 40 years of experience in the medical industry. He is president of Visionary Consulting LLC and has been consulting with medical OEM’s and CMOs for over 7 years. Mr. Braido’s has a broad breadth of medical industry experience in prototype/product development, global strategic/tactical planning, technical due-diligence/gap analysis for acquisitions, engineering, operations and business development. He has had great success working at Ethicon Endo-Surgery a J&J Company, Baxter Healthcare, Teleflex Medical, GW Plastics and The Tech Group with increasing responsibilities to the level of VP of Advanced Technologies. He was a member of the Board of Directors for the Society of Plastic Engineers Medical Division for over 10 years and elected Chairman of the Medical Division twice.
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
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Compliance Trainings
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Canada
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Email : support-AT-compliancetrainings.com