Health education online or at distance

ISO/IEC 17025:2017 Section 7 - Process Requirements and Section 8

Ref: 29652 Thursday June 20th, 2019 - Online

Overview: How does the new standard impact laboratories that are already accredited and how do you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits?   Why should you Attend: What are the changes to the technical and ...

Auditing Laboratories Conducting Assays Supporting Biologics

Ref: 29653 Thursday June 20th, 2019 - Online

Overview: Sponsors or consultants auditing labs on behalf of a pharmaceutical or biopharmaceutical company need strong tools for preparing and conducting audits.Careful consideration of the work that will be performed at the laboratory provides a working framework for the content of the ...

Excel Spreadsheet Validation for FDA 21 CFR Part 11 (2019)

Ref: 29654 Friday June 21st, 2019 - Online

Overview: These may be used for GxP regulated activities, and they present particular compliance challenges, as Excel and other spreadsheets are not originally designed for the regulated environment.   Why should you Attend: Part 11 / Annex 11 Computer Systems Validation (CSV) is to ...

Responsibility for Off-label Claims in Social Media

Ref: 29655 Tuesday June 25th, 2019 - Online

Overview: One big issue is how you patrol and control what someone else is saying about your product in a public forum. Once the off-label information is out there, what is scope your responsibility?   Why should you Attend: What is considered "off-label" Using social media website ...

Canadian Drug and Health Products Regulatory Landscape

Ref: 29656 Tuesday June 25th, 2019 - Online

Overview: The focus will be on drugs, biologics and medical devices, We will also be providing an overview of how the regulatory landscape is currently evolving for most efficient strategic planning.   Why should you Attend: This webinar will give you a snap shot of what is current, ...

Investigation and Root Cause Analysis to Meet FDA Expectations

Ref: 29657 Wednesday June 26th, 2019 - Online

Overview: This live interactive presentation will also discuss the regulations associated with the detection, correction and prevention of human errors in GMP manufacturing and laboratory processes.   Why should you Attend: We will focus on improved techniques to get to the real ...

FDA Inspections: From SOP to 483 in (2019)

Ref: 29658 Friday June 28th, 2019 - Online

Overview: Does the FDA call in advance or just show up at my door? Where do I let the inspector go? Do I give them a tour? What should I let them see? Who should I let them talk to? Are they ever going to leave?   Why should you Attend: This session will discuss how to prepare for ...

Machine Learning Tutorial for Beginner to Advanced Simpliv

Ref: 26894 03/28/2018 -> 12/31/2019 - Online

Machine Learning Tutorial for Beginner to Advanced Simpliv

The Complete Python 5 Course Beginner to Advanced Simpliv

Ref: 26895 03/28/2018 -> 12/27/2019 - Online

The Complete Python 5 Course Beginner to Advanced Simpliv

How does compliance with 21 CFR Part 11 help ensure data integrity and subject safety in clinical research

Ref: 27324 05/25/2018 -> 08/28/2020 - Online

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(ELECTRONIC RECORDS; ELECTRONIC SIGNATURES) and all of the ramifications of this Part of the code is essential. Basically elec

Advanced Spine Surgery in India

Ref: 29447 04/03/2019 -> 05/01/2020 - Online

Low Cost Spine Surgery in India