Technical Writing for Medical Products: SOPs, Investigations and Change Records training seminars presented by Online Compliance Panel register now on FindaSeminar.com

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Technical Writing for Medical Products: SOPs, Investigations and Change Records  

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Online Compliance Panel   

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This webinar is aimed at pharmaceutical and medical device professionals with scientific expertise

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Seminar Summary:

In this training program, attendees will learn quick formatting tips that will make writing more readable and learn how to use formatting tools in a way to maximize the impact of their writing in an electronic system. (see full course description)

 

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Training Course Syllabus:


Technical Writing for Medical Products: SOPs, Investigations and Change Records Webinar

Objectives of the Presentation

Learn some quick formatting tips that will make writing immediately more readable
Learn how to use formatting tools in a way to maximize the impact of their writing in an electronic system
Learn how to format SOPs to facilitate clarity
Learn how to document investigational information in a way that is understandable to non-technical professionals
Learn how to author change records that explain the rationale for change in clear, non-technical language

Why Should you Attend

Advanced technology may have pushed effective communication to the wayside to make clear writing a lost art, now due for revival. In the Information Age, a surplus of technical data proliferates with very little information communicated in plain language. Unclear communication can confuse compliance auditors who need to quickly assess whether an unfamiliar organization fulfills requirements. Poor writing therefore can contribute to an audit communication breakdown, leading to undesired audit findings.

This webinar will focus on effective communication of technical information so that an external auditor will quickly understand it and credit your organization with doing the job right.

Areas Covered

General technical writing guidelines
Tips to improve readability and understanding of your documents
Guidelines for SOP writing
Guidelines for writing investigation findings
Guidelines for writing change records
Proofreading your

Who will Benefit

This webinar is aimed at pharmaceutical and medical device professionals with scientific expertise, who struggle with documenting information so that it is understandable to non-technical professionals. Pharmaceutical and medical device professionals, Technicians taking on more authorship duties, Document authors, Investigators, Subject-Matter Experts wishing to share their knowledge, Medical writers and anyone who writes or want to write, Sponsors, Regulatory affairs personnel, Quality assurance personnel, Information technology personnel, Vice presidents, Directors and Managers, People interested in investing in the FDA-regulated

Seminar Summary:

In this training program, attendees will learn quick formatting tips that will make writing more readable and learn how to use formatting tools in a way to maximize the impact of their writing in an electronic system. (see full course description)

print this agenda print agenda for the Technical Writing for Medical Products: SOPs, Investigations and Change Records training seminar

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