Dublin, Nov. 10, 2026 (GLOBE NEWSWIRE) -- "Technical Writing for Med Devices, Pharma and Biotech (July 20th - July 23rd, 2026)" has been added to ResearchAndMarkets.com's offering.
Research and Markets has made the recording of “Technical Writing for Med Devices, Pharma and Biotech” available for on-demand purchase. The four-day virtual seminar, led by Charles H. Paul, was held live on July 20-23, 2026. It offers a structured approach to technical writing in the life sciences, moving from foundational principles to applied writing across regulated document types.
Key Event Facts
- Course: Technical Writing for Med Devices, Pharma and Biotech
- Format: Recorded training, accessed online through a secure website
- Original live event: July 20-23, 2026 (EST)
- Duration: Four days
- Speaker: Charles H. Paul
- Regulatory focus: FDA and ISO documentation expectations
Day 1: Foundations of Technical Writing in the Life Sciences
The seminar opens with the types of documents used across medical devices, pharma and biotech, and the regulatory expectations that govern them. Participants examine the consequences of poor writing and what separates effective documents from ineffective ones.
Day 2: Audience, Structure and Information Development
Day 2 focuses on analysing audience needs and capability, setting the right level of detail and language, and writing for non-native readers. It also covers structuring and organising documents for both usability and compliance.
Day 3: Working With SMEs and Writing Regulated Documents
Participants learn how to interview and work with subject matter experts (SMEs), observe and document processes, and manage conflicting input. The day then applies these skills to investigations and deviations, standard operating procedures (SOPs) and work instructions, and regulatory submissions.
Day 4: Writing Mechanics, Simplification and Finalization
The final day covers grammar, punctuation and consistency rules, active versus passive voice, and techniques for removing ambiguity and simplifying text. It closes with reviewing and editing, incorporating reviewer comments, resolving disagreements between reviewers, and managing document approval and timelines.
Why You Should Watch
- Write SOPs, work instructions, investigations and regulatory submissions that meet FDA and ISO expectations
- Match detail, structure and language to the audience, including non-native readers
- Extract accurate information from subject matter experts and manage conflicting input
- Remove ambiguity with proven simplification and writing-mechanics techniques
- Run review cycles, resolve reviewer disagreements and keep document approvals on schedule
Featured Speaker
- Charles H. Paul
Life sciences professionals responsible for regulated documentation can purchase the recording through Research and Markets. Access details are sent by email.
For more information about this training visit https://www.researchandmarkets.com/r/itcjaj
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