Past Events (3,027)

Webinar On "Building Your Company FDA FSMA Preventive Control Food Safety Plan "

January 16, 2018 from 1pm to 2pm – Online Description : All food facilities registered with the United States Food and Drug Administration (FDA) must comply with the requirements under the Food Safety Modernization Act (FSMA) to develop and… Organized by Sam Miller | Type: online, /, webinar
Which data and systems are subject to Part 11

January 16, 2018 from 10am to 11:30am – Fremont Overview: This webinar details the regulation and how it applies to computerized systems. Learn exactly what is needed to be compliant for all three primary areas: SOPs for the IT infrastructure, ind… Organized by Event Manager | Type: online

What is Project Management in Pharmaceutical Industry Seminar

January 15, 2018 at 9am to January 16, 2018 at 6pm – San Diego, CA Course "Risk Based Project Management for the Life Sciences Industry" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.… Organized by NetZealous DBA as GlobalCompliancePanel | Type: regulatory, and, compliance, seminars

Clinical Data Systems Regulated by FDA

January 12, 2018 from 10am to 11:30am – Fremont 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 b… Organized by Event Manager | Type: online
The Value of a Human Factors Program

January 12, 2018 from 10am to 11am – Fremont Overview: This webinar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program. Why should you… Organized by Event Manager | Type: online

Medical Device MDR following new FDA Guidance

January 11, 2018 from 1pm to 2pm – Online Description : This webinar explains the MDR regulation considering the new information contained in the Guidance and describes a compliant MDR procedure. Areas covered will include reporting requ… Organized by Sam Miller | Type: webinar
What is Process Validation Report | 21CFR11 Compliance Checklist 2018

January 11, 2018 at 9am to January 12, 2018 at 6pm – Germany Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completio… Organized by NetZealous DBA as GlobalCompliancePanel | Type: regulatory, and, compliance, seminars

Webinar On "Supplier Quality Management Utilizing Principles of Lean Documents and Lean Configuration"

January 9, 2018 from 1pm to 2:30pm – Online Description : All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form… Organized by Sam Miller | Type: online, /, webinar
Ensuring Data Integrity and Safety in Clinical Research

January 9, 2018 from 10am to 11am – Fremont Overview: Electronic medical records and electronic handling of study data is increasingly common. To involve computer systems in clinical research implies knowledge of 21 CFR Part 11. Why should you… Organized by Event Manager | Type: online

Act for Transportation and Logistics Professionals

January 8, 2018 from 10am to 11am – Fremont Overview:The FSMA is paradigm shift that moves the focus from food inspections to preventative measures and process compliance. Why should you Attend:Specific provisions of the FSMA that impacts tran… Organized by Event Manager | Type: online