Live Webinar Medical Device Trends for Computer Systems Regulated by FDA

01:00 PM EDT | 10:00 AM PDT | 12:00 PM CDT Duration 60 Minute

Webinar Includes : All the training handouts , certificate ,Q/A and 60 mins Live Webinar


The Webinar will focus on the importance of managing FDA oversight of computer system validation in the medical device industry by anticipating and preparing for trends. The type and extent of oversight varies with changes to the economic, political, and business environment. FDA funding, the length of government reach into the private sector, and the ability of companies to lobby the government for less regulation all play a role in terms of the dynamics at play between industry and the FDA.
Medical device companies must be vigilant in understanding the factors that impact their ability to operate with oversight from FDA as it relates to computer system validation. In all cases, companies should do the right thing and have robust computer system validation programs that are well executed and documented. However, there are some extremes in oversight that occasionally crop up and may cause expectations to go above and beyond what is considered reasonable. In such cases, companies must determine how much risk to take in terms of the strength of their programs, and how well they are able to negotiate with their FDA auditors.
Typically, a medical device company will develop a relationship with the FDA office that sends auditors to oversee computer system validation programs in their organization.

Depending on upcoming trends, medical device companies may want to work harder to further strengthen these relationships and build greater trust with FDA

Why Should You Attend

Effective and compliant computer system validation is critical to any medical device organization. With changes in the economic, political and business factors that influence the extent to which FDA exercises oversight, companies must actively anticipate what that means for their existing and planned computer system validation programs and plans.
It is vital for medical device companies to maintain a pulse on the regulatory environment in order to fortify system validation efforts, as necessary, to meet FDA expectations. Conversely, they must be vigilant to not allow looser regulations or oversight to influence the level of computer system validation they adopt as their standard practice. There is always danger that a medical device company will become too lax, and will either be caught off-guard, or used by FDA to make an example of why they need more resources and need to tighten those very regulations. All in all, it is the best practice to have a robust computer system validation, continue executing against it consistently, and documenting it thoroughly.

Areas Covered

•   Describe some of the key factors that influence the degree of FDA oversight for computer system validation programs in the medical device industry
•   Discuss how to anticipate and understand trends in FDA oversight of the medical device industry, as they begin to emerge
•   Discuss ways for medical device companies to build a solid relationship with FDA and leverage it to gather information about emerging trends
•   Discuss ways that medical device companies can adjust their computer system validation programs to changes in the regulatory environment
•   Discuss ways to apply basic computer system validation principles to ensure that in all cases a medical device company is prepared for emerging trends
•   Provide examples of changes to the factors influencing the regulatory environment and how medical device companies have reacted or responded
•   Discuss some of the unnecessary risks medical device companies have taken in response to changes in the regulatory environment and the ramifications

Who will Benefit

Any other FDA-regulated industry, plus any Life Science Consulting or Contracting firm
•   Information technology analysts
•   QC/QA managers and analysts
•   Compliance managers
•   Lab managers
•   Automation analysts
•   Computer system validation specialists
•   GMP training specialists
•   Business stakeholders and individuals who are responsible for computer system validation planning, execution, reporting, compliance, and audit
The webinar should target consultants working in the life sciences industry who are involved in computer system implementation, validation and compliance.

Industries who can attend

Primarily Medical Device Industry, but professionals in the following industries may also benefit from the content:
•   Pharmaceutical
•   Medical Diagnostics
•   Biotechnology
•   Tobacco and Related (Vapor, e-Cigarette, Cigar, etc.)
•   Animal Health
•   Medical Device Manufacturers
•   Medical Device Software Manufacturers

Speaker Profile

Carolyn Troiano

Carolyn Troiano has more than 35 years of experience in the tobacco, pharmaceutical, medical device and other FDA-regulated industries.   She has worked directly, or on a consulting basis, for many of the larger pharmaceutical and tobacco companies in the US and Europe, developing and executing compliance strategies and programs

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