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Creating Reader-Focused Technical Documents in FDA Regulated Industries


Monday, December 5, 2016 at 8:30 AM - Tuesday, December 6, 2016 at 4:30 PM (EST)

Creating Reader-Focused Technical Documents in FDA...

Ticket Information

Ticket Type Sales End Price Fee Quantity
Seminar One Registration (Early bird price)
For Registrations after November 20, 2016 - $1699
Dec 5, 2016 $1,299.00 $0.00
Seminar One Registration Dec 5, 2016 $1,699.00 $0.00

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Event Details

Course Description:

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 your reader, who needs to use the information to make critical decisions in a manufacturing environment for products that have life-and-death consequences. Poor writing can therefore not only contribute to poor communication, but to human survival.

This seminar will focus on effective communication in technical documents. While true that effective communication is essential for auditors to assess your regulatory compliance, it is more important that clear documentation can improve the safety of the products you work hard to produce. Rather than focusing on what information to include in technical writings, focus on your reader, who must understand the intended message.

In this two-day workshop, you will learn how to structure a technical document with the reader in mind. You will learn how to paint a mental picture of the content, to enhance reader understanding. Participants should bring an in-process technical report to the workshop, to immediately yield business outcomes.

Learning Objectives:

The workshop objectives are to help technical writers:

  • Plan and write consistent, reader-focused reports and other technical documents.
  • Write in a style that is clear and concise.
  • Develop content with a bottom-line message at the top, and main points that stand out and are reinforced with appropriate data.
  • Use Professional Touch tools that help build working relationships with readers.
  • Develop writing that groups content into digestible chunks to improve reading comprehension.
  • Work on a technical writing piece brought from the workplace to immediately apply the skills.


Who Will Benefit:

Anyone working in regulated environments for pharmaceuticals, medical devices, foods or dietary supplements can improve technical writing skills. Affected job titles range from entry-level employees to managers, and include individuals with the following job titles:

  • Document Control Specialists
  • Software Specialists
  • Quality/R&D Technicians
  • Quality/Production Supervisors
  • Technical Specialists
  • Quality/Technical Investigators
  • Compliance Professionals
  • Manufacturing/Production/Design Engineers
  • Process Owners
  • Quality Engineers/Auditors


For Registration -           


Note: Use coupon code < NB5SQH8N > and get 10% off on registration.

Have questions about Creating Reader-Focused Technical Documents in FDA Regulated Industries? Contact ComplianceOnline

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When & Where

Research Triangle Park

Durham, NC

Monday, December 5, 2016 at 8:30 AM - Tuesday, December 6, 2016 at 4:30 PM (EST)

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Enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality & safety.

Making sure that we are responsible corporate citizens helping our constituents build a more responsible enterprise, one which operates with high quality , under a code of ethics, and with process discipline to ensure greater shareholder returns.

Keeping things simple and straight forward , so that we all can indeed improve the quality of our processes, our work, our businesses and enhance compliance globally.

Being inclusive, giving the process experts ( & novices! ), compliance professionals, quality champions, and regulatory agencies a voice so that all of us can contribute and make a difference.

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Creating Reader-Focused Technical Documents in FDA Regulated Industries
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