ComplianceGrowth | Train online from leading industry experts

Carolyn Troiano

Biography:

Carolyn Troiano has more than 35 years of experience in computer system validation and compliance in the pharmaceutical, medical device, 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.

Live Business Training Events

No Live Training available.

Featured OnDemand Webinars

21 CFR Part 11, FDA's Guidance for Electronic Records and Signatures Using a Computer System Regulated by FDA

Duration: 90 Minutes
| Pharmaceutical
| All Days

GAMP®5, Second Edition and Alignment with FDA’s Draft Guidance for Computer Software Assurance (CSA)

Duration: 90 Minutes
| Pharmaceutical
| All Days

Cybersecurity in Medical Devices: Quality System Considerations and Content of Premarket Submission

Duration: 60 Minutes
| Pharmaceutical
| All Days

Risk-Based Approach to Validating IT Infrastructure Used for FDA-Regulated Systems

Duration: 90 Minutes
| Pharmaceutical
| All Days

CSV vs. CSA: Aligning the Agile Methodology to the GAMP 5 “V” Model and SDLC Methodology

Duration: 90 Minutes
| Pharmaceutical
| All Days

Update to FDA's Draft Guidance on 21 CFR Part 11, Electronic Records/Signatures Used for Clinical Investigation

Duration: 90 Minutes
| Pharmaceutical
| All Days

Strategies for Effective Risk Management in FDA IT Infrastructure Validation

Duration: 90 Minutes
| Pharmaceutical
| All Days

Computerized Systems Validation, Data Integrity & Cloud Computing In Pharma & Biotech

Duration: 720 Minutes
| Pharmaceutical
| All Days

Un-Subscribe

To Unsubscribe You have to email us your email id via which we will first verify your account and then you will be un-subscribed. All work will be done From our end.

Enter Your Email id....

Carolyn Troiano

21 CFR Part 11, FDA's Guidance for Electronic Records and Signatures Using a Computer System Regulated by FDA

GAMP®5, Second Edition and Alignment with FDA’s Draft Guidance for Computer Software Assurance (CSA)

Cybersecurity in Medical Devices: Quality System Considerations and Content of Premarket Submission

Risk-Based Approach to Validating IT Infrastructure Used for FDA-Regulated Systems

CSV vs. CSA: Aligning the Agile Methodology to the GAMP 5 “V” Model and SDLC Methodology

Update to FDA's Draft Guidance on 21 CFR Part 11, Electronic Records/Signatures Used for Clinical Investigation

Strategies for Effective Risk Management in FDA IT Infrastructure Validation

Computerized Systems Validation, Data Integrity & Cloud Computing In Pharma & Biotech

Un-Subscribe

hJHoaX

Speaker Opportunity

Suggest a Topic

Carolyn Troiano

Live Business Training Events

Featured OnDemand Webinars

21 CFR Part 11, FDA's Guidance for Electronic Records and Signatures Using a Computer System Regulated by FDA

GAMP®5, Second Edition and Alignment with FDA’s Draft Guidance for Computer Software Assurance (CSA)

Cybersecurity in Medical Devices: Quality System Considerations and Content of Premarket Submission

Risk-Based Approach to Validating IT Infrastructure Used for FDA-Regulated Systems

CSV vs. CSA: Aligning the Agile Methodology to the GAMP 5 “V” Model and SDLC Methodology

Update to FDA's Draft Guidance on 21 CFR Part 11, Electronic Records/Signatures Used for Clinical Investigation

Strategies for Effective Risk Management in FDA IT Infrastructure Validation

Computerized Systems Validation, Data Integrity & Cloud Computing In Pharma & Biotech

Instant Discount

Purchase any WEBINAR and get $30 OFF

Un-Subscribe

hJHoaX

Speaker Opportunity

Suggest a Topic

Subscribe Upcoming Updates