Training Program Title

Key Considerations for Regulatory Compliant Document Storage

Contributor

Forte MarketingFollow

CTSA Hub Administered

no

Contact Information

marketing@forteresearch.com

Training Program Description

The criteria covered in 21 CFR Part 11 are not the only requirements that should be considered for compliant document management associated with clinical trials.

Competency Keywords

Clinical research, Clinical trial

Other Keywords

21 CFR Part 11, Document Management

Digital Commons Disciplines

Medical Education

Public

yes

Cost to Access

no

Competency Domains

Study and Site Management

Delivery Method

Online

Target Learners

Principal Investigators; Clinical Research Professionals (other than PI)

Learning Level

Fundamental

Frequency

On demand

Associated Assessment

no

Share

COinS