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What Are The Main Benefits Of POWER OF SHAREPOINT

Author: Adam Fleming
by Adam Fleming
Posted: May 02, 2019

SharePoint is now almost the accepted and standard mode for organizations to share relevant information and files with other people, both in the company and outside.

The main benefits of SharePoint will be explained at a sixty-minute webinar that Compliance4All, a leading provider of professional training for all the areas of regulatory compliance, is organizing on April. Tom Fragale, a Microsoft Certified Trainer and a Microsoft Certified Expert in Excel, will be the speaker at this session. Please visit https://www.compliance4all.com to enroll for this valuable session.

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The main focus of learning from this webinar on the main benefits of SharePoint will be the ways of setting up and managing a SharePoint team site. Tom will teach participants the meaningful ways by which they can put the various features of SharePoint to add their company logo and colors, pages, and users, create links, set up document folders, share the site, add other apps to their site, and to customize their site, among other topics of learning.

In essence, at this webinar on the main benefits of SharePoint, participants will learn how to set up their own SharePoint site and manage it effectively. This webinar will be of great use to anyone who is in charge of a SharePoint site, or will need to be, in the future. Tom will cover the following areas at this webinar:

  • SharePoint overview
  • Screen tour
  • Adding logos and colors to your site
  • Adding users
  • Adding groups
  • Adding apps to your site
  • Setting up your links
  • Adding and changing pages
  • Setting up your document libraries
  • Uploading and Downloading documents.

Business Owners, CEO’s/CFO’s/CTO’s, Managers of all levels, anybody with large amounts of data, anybody who uses SharePoint on a regular basis, and wants to be more efficient and productive, Accountants, CPA’s, Controllers, Financial Consultants, IT professionals, Auditors, Human Resources Personnel, Bookkeepers and Marketers will gain tremendously from this session.

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About the speaker:

Dr. Laura Brown, PhD, MBA, Diploma Clinical Sciences, is an independent QA and training consultant in the pharmaceutical industry. She is a managing director with LB Training and Development Ltd., course director for the M.Sc. in Clinical Research, School of Pharmacy at the University of Cardiff, and course director for M.Sc. Regulatory Affairs, TOPRA. Dr. Brown has 20 years experience running clinical trials and clinical quality assurance in the pharmaceutical industry, and auditing clinical trials internationally. She has held a number of international and senior management QA positions in the pharmaceutical industry including her role as an associate director with a leading GCP audit consultancy.

She has worked for several international companies like GlaxoWellcome, Hoechst Marion Roussel and Phoenix International. Dr. Brown has published material on the new EU Clinical Trial Regulation and also a practical guide to the current regulatory requirements for carrying out clinical trials in the EU. She has penned a chapter on training QA staff in the leading GXP book "Good Clinical, Laboratory and Manufacturing Practices" (2007). She has authored SCRIP’s latest GCP guide and one entitled "Practical Guide to the Clinical Trial Directive". She is also co-author of several books including "Developing the Individual" and "Project Management for the Pharmaceutical Industry". She has regularly lectured at conferences and in training courses on QA and GXP issues.

Dr. Brown developed an e-learning module: "How to Prepare for Audit and Inspection" for Zenosis (a regulatory commercial e-learning training organization) in 2008 and is editor of an e-learning SOP series for Henry Stuart Conferences (2013). She runs many training courses on topics such as: pharmaceutical project management, understanding the pharmaceutical industry/drug development, writing and managing SOPs, GCP, regulatory requirements for clinical trials, the clinical trial directive, managing clinical trials, QA management and business skills, how to prepare for audit and inspection, how to audit, etc.

About the Author

Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations.

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Author: Adam Fleming

Adam Fleming

Member since: Jul 14, 2017
Published articles: 87

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