Checkbox

Technical Writing Workshop Focuses on Key Elements for Lifescience Companies

By MedTech Intelligence Staff
No Comments
Checkbox

This two-part virtual workshop will guide participants through the process of how to write effective documents.

Mark Proulx, MLB Consulting Services
Mark Proulx, president of MLB Consulting Services

Technical writing is not as easy as it sounds—especially for professionals in the lifescience space. MedTech Intelligence is offering a Technical Writing Virtual Workshop for professionals who are in the medical device, pharma, pharmacy, and biologics corporate world.

The virtual workshop takes place over two two-hour sessions on March 3 and March 10 (12 pm – 2pm ET).

The course will be instructed by world-class, international quality and regulatory consultant Mark Proulx, president of MLB Consulting Services. Proulx has more than 25 years of direct manufacturing, auditing, and FDA experience and is a certified quality auditor and Six Sigma Black Belt.

The workshop was developed for the following industry professionals:

  • Engineers responsible for writing up investigations and reports
  • Tech writers who must communicate the results of testing in reports, write up papers, produce arguments for or against an issue
  • Middle-level managers who are attempting to make arguments or show results
  • Laboratory staff who document results and write reports
  • Technicians who must write up test protocols, non-conformance reports, corrective actions, reports to upper management, etc.
  • Quality Assurance/Quality Control and Regulatory Compliance people who must document clearly the purpose of investigations and produce final reports that clearly state actions to be performed or the results of testing

Learn more about this special Technical Writing Virtual Workshop now! Register by Tuesday, February 11 for a special discount.

Related Articles

  • RQM plus logo

    Jordi labs and its team of Ph.D. analytical chemists developed a proprietary, multi-detector approach to ensure that all extractables are accurately characterized to comply with global materials testing regulatory requirements.

  • MedTech Regulatory Intelligence Summit

    Registration is now open for the MedTech Regulatory Intelligence Summit in Washington, DC, May 16-17. Join us as we take a closer look at strategies and best practices in developing an effective and sustainable regulatory strategy for today’s global market.

  • MedTech Regulatory Intelligence Summit

    On May 16-17, device developers, regulatory affairs and regulatory intelligence professionals will come together in Washington, DC, for two days of education, discussion and networking to share strategies and best practices on navigating current and on the horizon regulatory requirements.

  • FDA Logo

    The FDA is seeking input from organizations interested in collaborating with the agency on the development and execution of the medical device active surveillance system, which is focused around achieving better data capture and detection of potential safety signals in…

Leave a Reply

Your email address will not be published. Required fields are marked *