Medical Writing Path 1 |  Medical Communications

Knowing the basics of writing scientific texts

1.”Medical Writing Course: Improve your Writing & Reviewing Skills”

Training Duration: 3 modules of 2 hours each (6 hours in total)
Dates: 15th, 17th and 19th March 2021; 10:30 am – 12:30 pm CET

The aim of this course is to improve medical writing skills & the quality of texts that you regularly prepare or review. Whether your text is an email, laboratory report, summary, regulatory submission, manuscript or business proposal, learn to make your message effective.

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Appropriately approach the strategic Publication Planning

2.”7-Step Workshop to Master your Publication Planning”

Training Duration: 2 modules of 3.5 hours each (7 hours in total)
Dates: 08th and 09th April 2021; 9:30 am – 1:00 pm CEST

In this workshop the key aspects and challenges of Publication Planning will be explored to give insights on what publication planning is, the importance of good publication planning and how the different figures involved in the development of disclosures can work together to succeed.
Maximize the impact of:
▪ Scientific manuscripts in peer-reviewed journals
▪ Data presented at congresses
▪ Data published on clinical trial registries
▪ Data included in Clinical Study Reports
▪ Data shared through social media

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The basics for writing a scientific paper

3.”Writing Scientific Articles: Starting with the Right Foot”

Training Duration: 4 modules of 2 hours each (8 hours in total)
Dates: 10th, 11th, 12th and 17th May 2021; 2:00 pm – 4:00 pm CEST

This workshop will help you start writing scientific articles for peer-reviewed journals in the right way, effectively communicate your findings and conclusions and optimise the writing process.
Attendees will benefit from the perspective and experience of two international experts in writing scientific papers and their management. Between them, they have successfully published many hundreds of articles across a wide variety of scientific and clinical specialties.

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Medical Writing Path 2 | Regulatory Writing

What are the characteristics of good quality technical/scientific documents?

1.”Tips and Tricks to Improve your Technical/Scientific Writing”

Training Duration: 3 modules of 2 hours each (6 hours in total)
Dates: 27th, 28th and 29th September 2021; 2:30 pm – 4:30 pm CEST

How can we prepare documents that please our audience? Are there general rules that might help us effectively write any type of technical/scientific documents?
This course will answer those questions and more, putting you on the right path to become a skilled and successful writer. Through exercises and discussion, you will learn fundamental techniques that will allow you to prepare high quality documents.

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The importance of the protocol as the central document for a study

2.”Clinical Study Protocols – Structure & Content”

Training Duration: 3 modules of 3.5 hours each (10.5 hours in total)
Dates: 06th, 07th and 08th October 2021; 9:30 am – 1:00 pm CEST

The study protocol is the foundation of any clinical research and a key factor in the success of its conduction. This course will give you an insight into the importance of study protocols as core documents of any clinical study. We will discuss the essential elements, the structure and its content with a hands-on practical approach.

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The final step…preparing a good quality Clinical Study Report!

3.”Clinical Study Reports – a 360° Perspective”

Training Duration: 2 modules of 3 hours each (6 hours in total)
Dates: 27th and 28th October 2021; 9:30 am – 12:30 pm CEST

This virtual course in 2 sessions covers scheduling, managing and authoring of clinical study reports (CSRs) for modern design clinical studies. It discusses the stages of preparation of CSRs in the context of precursor documents including the clinical study protocol (CSP), the statistical analysis plan (SAP), and the incorporation of study data. Components of the integrated CSR include narratives and appendices, and the preparation of these sections of the CSR will also be covered. Scheduling an achievable reporting timeline for this complex and multi-component document will be explained.

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