Overview:
The
California Privacy Rights Act (CPRA) passed by voters in 2020 came into effect
on January 1, 2023. It is considered to be an amendment to the California
Consumer Privacy Act (CCPA). In this webinar, we will discuss the key changes
to California’s landmark CCPA that included in the CPRA and what businesses
have to do to comply with the law.
We
will discuss the differences between the CCPA and the CPRA, which adds some
consumer rights in California. All of the consumer rights extended by both the
CCPA and the CPRA will be delineated and explained. The CPRA also defines what
is meant by a business, service provider, contractor, and third party. Further,
it defines what is meant by the sale of personal information, the sharing of
personal information, and sensitive personal information.
We
will also discuss the thresholds required for the CPRA to be applicable to a
company, and if it does apply, how a company can prepare by making any
necessary policy or procedural changes in order to comply.
During
this webinar, we will also cover the Health Information Portability and
Accountability Act (HIPAA) in the US and the General Data Protection Regulation
(GDPR) that is in effect to protect citizens’ personal data when they reside in
the European Union (EU). We will compare and contrast these with the CPRA,
providing specific requirements and how industry subject to these regulations
can meet compliance.
Areas
covered during the session:
- The
California Privacy Protection Act (CPPA)
- The
California Privacy Rights Act (CPRA)
- New
consumer rights extended to those residing in California through the amended
CPPA, or CPRA
- Enforcement
obligations for the CPPA and CPRA
- The
California Privacy Protection Agency, newly created as part of the CPPA
- Delineation
by thresholds of which companies operating in California are obligated to
comply
- Specific
obligations of companies that are subject to CPPA and CPRA
- Actions
companies may take to ensure compliance with the CPPA and CPRA
- Definitions
of sale, sharing, and related terms intended to describe actions by a company
related to a consumer’s personal information
- Privacy
policies and procedures to be considered by companies obligated to comply
- Actions
consumers may take in a case where a company misuses their personal information
or otherwise fails to comply with CPPA and/or CPRA
- Health
Information Portability and Accountability Act (HIPAA)
- General
Data Protection Regulation (GDPR)
- Q&A
Why
should you attend?
Any company that does business in the state of California must understand the rules that would force them to comply with both the CCPA and the CPRA amendment to it. Knowing whether these apply to your company is critical in order to fully prepare and be in compliance by July 2023, as any company doing business in California and meeting the thresholds described must comply by that date. This may mean a change to existing policies and procedures, and creating any necessary mechanisms for handling personal information of California residents in compliance with the rule.
Companies
doing business in the US must also adhere to the HIPAA regulation, and those
companies that hold personally identifiable data of individuals residing in the
EU must meet the GDPRs.
We
will discuss the specifics about these three regulations, indicating how they
are similar and dissimilar, and the requirements that must be met.
It is
important to know whether CPPA, CPRA, HIPAA, and/or GDPRs apply to your
company, what obligations you may have imposed on your company as a result, and
what you must do to comply with these.
What
industries will benefit from your training?
Social
Media, Sales & Marketing, Government, Manufacturing, Testing, Packaging and
Distribution companies in the following industries that are regulated by FDA
are required to follow GxPs:
- Pharmaceutical
(for drug/tobacco/e-liquid products introduced using a medical device)
- Medical
Device, where there is integration with e-liquid and/or tobacco products
- Tobacco
(based on the Tobacco Control Act of 2009)
- E-Liquid/Vapor
(based on the “Deeming” Act of 2016)
- E-Cigarette
(based on the “Deeming” Act of 2016)
- Cigar
(based on the “Deeming” Act of 2016)
- Third-Party
companies that support those in the above industries, whether partnering or
consulting
Who
will benefit?
Personnel
in the following roles will benefit:
- Information
Technology Analysts
- QC/QA
Managers
- Retailers
- Marketers
- Sales
Managers
- Publishers
- Editors
- Website
Administrators
- Legal
Professionals
- Regulatory
Professionals
- Government
Agencies
- Clinical
Data Managers
- Compliance
Managers
- Manufacturing
Managers
- Supply
Chain Specialists
- Business
Stakeholders responsible for data privacy
- Consultants working in the life sciences industry who are involved in assuring data privacy
- Auditors engaged in the internal inspection of records and practices related to privacy data
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. She is currently an independent consultant, advising companies on computer system validation and large-scale IT system implementation projects.
During her career, Carolyn worked directly, or on a consulting basis, for many of the larger pharmaceutical companies in the US and Europe. She developed validation programs and strategies back in the mid-1980s, when the first FDA guidebook was published on the subject, and collaborated with FDA and other industry representatives on 21 CFR Part 11, the FDA’s electronic record/electronic signature regulation.
Carolyn has participated in industry conferences. She is currently active in the PMI, AITP, and RichTech, and volunteers for the PMI’s Educational Fund as a project management instructor for non-profit organizations.
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Tags: Data Privacy, CPRA, HIPAA, GDPR, Compliance, Carolyn, Troiano, April 2023, Webinar