How to Train Yourself to be a Good Technical Writer
Date: January 22, 2025
Duration: 60 Minutes
Time: 12 PM EST
This webinar, presented by a leading technical writer with thousands of well-received documents, will discuss self-training and evaluation skills for professionals in the FDA-regulated industry. The core competencies developed using these tips can be applied to other industries as well. The presenter will share his tips for identifying your writing styles, industry standards for different kinds of documents, and how to find free or inexpensive resources to polish ones skills. The seminar will also discuss numerous opportunities from your daily life that can be used to create writing samples, present your documents to peers, and get critical evaluation for further improvement. Techniques for group-writing, contract writing, ghost writing, and several other practices common in the regulated industry will be discussed. This one-of-a-kind seminar is designed to provide a well-rounded training to all future and current technical and even non-technical writers, who want to develop and improve their writing skills.
- Basic rules and skills required for technical writers
- Different categories for documents and the desired skills for each
- Common opportunities that are often overlooked or under-estimated by aspiring writers
- FDA expectations for quality of written text in submitted documents
- Balancing writing for fun and as a job
- Everyone can write philosophy of training new writers
- Best practices for setting expectations from writers
- Dos and don’ts for self-evaluation, critiquing other writers, corrections and improvements
- Group-writing, contract writing, ghost writing, and several other practices
- Native and non-native writers in English and other languages
- 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 industry
Speaker: Mukesh Kumar
PhD, RAC | CEO, FDAMap
For more info, fill the box below. We will contact you within 24 hrs.
Webinar Fee
Prices are in US Dollars.
The registration fee includes: The live webinar & all related course materials.
Terms & Conditions to register for the Webinar
Your Registration for the workshop is subject to following terms and conditions. If you need any clarification before registering for this webinar please email us at info@fdamap.com
Payment
We accept credit card, debit card, and PayPal.
Cancellations & Substitutions:
Written cancellations through fax or email (from the person who has registered for this conference) received at least 5 business days prior to the start date of the event will receive a refund — less a $30 administration fee. No cancellations will be accepted — nor refunds issued — within 5 business days before the start date of the event. You may however, choose to substitute the webinar for which you are registered with some other webinar in the future.
On request by email or fax (before the seminar) a credit for the amount paid minus administration fees ($30) will be transferred to any future FDA Map event and a credit note will be issued. No-shows will be charged the full amount.
Webinar material will be uploaded on the website 24 hours before the scheduled date of the webinar. In case it is not available on the website due to some technical issues, we will email the material a few hours before the start of the webinar.
In the event FDA Map cancels the webinar, FDA Map will issue a full refund to all the registrants for that webinar. Some topics and speakers may be subject to change without notice.
