This technical writing training program will offer attendees an understanding of how the reporting process supports products in research, development, and in the marketplace. This virtual session will highlight the mandates for documentation set forth by the regulators, such as the FDA, the ISO, and other governing bodies. The program will train attendees on effectively reviewing and revising documents and assessing your audience, in effect producing effective written correspondence. (from )

complianceonline.com/technical-writing-for-the-pharmaceutical-medical-device-and-biotech-industries-webinar-training-704531-prdw

• February 10 from 10:00 am to 12:00 pm

  February 10, 2025 10:00 to February 10, 2025 12:00
• Online Event
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• Contact Sahitya for more information
  +1-888-717-2436 or [email protected]
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