21st Century Cures Act -New Guidance on Medical Device Software Compliance

01:00 PM ET | 10:00 AM PT | 12:00 PM CT Duration 90 Minutes

Webinar Includes : All the training handouts , certificate ,Q/A and 90 mins Live Webinar

"Carolyn Troiano has more than 35 years of experience in computer system validation in the pharmaceutical, medical device, animal health, tobacco and other FDA-regulated industries"

Waive the requirement for “informed consent” in specific cases

Description

The 21st Century Cures Act is a United States law enacted by the United States Congress in December 2016. It authorized $6.3 billion in funding, mostly for the National Institutes of Health (NIH). The act was supported by large pharmaceutical manufacturers and was opposed especially by many consumer organizations.

The intent of the Act is to streamline the drug and device approval process and bring treatments to market faster. Many fear that this will allow drugs and devices to be approved on weaker evidence, bypassing randomized, controlled trials, and bring more dangerous or ineffective treatments to market.
The bill incorporated the Helping Families In Mental Health Crisis Act, which increased the availability of psychiatric hospital beds and care.
The 21st Century Cures Act designated $1 billion in grants for states over two years to fight the opioid epidemic, which is surging in the US. The money may be used to improve prescription drug monitoring programs to make treatment programs more accessible, to train healthcare professionals in best practices of addiction treatment, and to research the most effective approaches to prevent dependency.

The 21st Century Cures Act modified the FDA Drug Approval Process. It was intended to expedite the process by which new drugs and devices are approved by easing the requirements put on drug companies looking for FDA approval on new products or new indications on existing drugs. Under certain conditions, the act allows companies to provide "data summaries" and "real world evidence" such as observational studies, insurance claims data, patient input, and anecdotal data rather than full clinical trial results.

The 21st Century Cures Act allows researchers to waive the requirement for “informed consent” in specific cases where the devices being tested don't pose any health risks beyond those of normal everyday life and wouldn't direct a patient's care in any way. However, researchers will still need to obey standard research protocols including Institutional Review Boards (IRBs) to approve their research design and ethics.

Why should you attend

Providing safe and effective drugs and medical devices is in the best interests of all those involved in the development, manufacturing, testing, and distribution of these products. In the case of the opioid epidemic, there is great interest in providing better medications and healthy pathways for treatment. This webinar will help explain how the 21st Century Cures Act will impact the current pharmaceutical and medical device industries, particularly their processes for new product and new product indication requests.

Areas Covered

Anyone working in the pharmaceutical and medical device industries who engage in research, development, testing, manufacturing, and supply chain functions will benefit from this presentation.

•        The 21st Century Cures Act
•        New processes for expediting drug and medical device approval for new products and new product indications
•        How to prepare for the Act
•        Industry Best Practices
•        Q&A

Who will Benefit

Professionals in the following industries may also benefit from the content:
•        Pharmaceutical
•        Medical Device
•        Biotechnology
•        Tobacco and Related (Vapor, e-Cigarette, Cigar, etc.)
Any other FDA-regulated industry, plus any Life Science Consulting or Contracting firm
•        Information technology managers and analysts
•        QC/QA managers and analysts
•        Clinical data managers and scientists
•        Compliance managers
•        Lab managers and staff
•        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
•        Consultants working in the life sciences, tobacco and related industries who are involved in computer system              implementation, validation and compliance
•        Anyone involved in the planning, execution, and reporting of a clinical trial (sponsor, director, researcher,                    regulatory role, etc.)

Industries who can attend

This 90 minute online course is intended for professionals in the Pharmaceutical and Biopharmaceutical Industry. Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel.


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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