Netzealous LLC DBA - Compliance4All, Online
2018-01-12
Overview: Companies engaged in the conduct of human clinical trials must adhere
to specific government regulatory requirements.Certain documents,
content and images related to a clinical trial must be stored and
maintained, and depending on the regulatory jurisdiction.
Why should you Attend: You should attend this webinar if you are responsible for establishing or
maintaining a TMF, or providing quality assurance for data included in
the file. This webinar will also benefit those involved in the conduct of
clinical trials, audit and inspection of clinical trial study data and
records, and submission of filings to regulatory agencies that involve
clinical trial data.
Areas Covered in the Session: Learn what content is required for a TMF for a clinical tria Learn about best practices and industry standards Understand the importance of developing an effective Standard
Operating Procedure
Who Will Benefit: T Support Staff QC/QA Managers and Analysts Clinical Data Managers and Scientists Compliance Managers and Auditors Lab Managers and Analysts Computer System Validation Specialists GMP Training Specialists
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com
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