Patient Information documents aimed to equip the general public with all relevant information about the healthcare journey, from making an informed decision about participating in a clinical trial to understanding the relevant information about drug's usage and potential side effects. The language should be simple and direct, avoiding complex medical and scientific details, but without oversimplifying the information. This will ultimately empower people/patients/subjects to reach well-informed conclusions.

A Protocol Amendment is a formal document intended to update or modify an existing CSP. Sometimes, adjustments are needed during the course of a trial to ensure it remains on track while maintaining participants’ safety and reliability of the results. It is paramount to provide a clear justification and to communicate any change unambiguously, that’s why we meticulously record each update, ensuring that information is readily available to support an uncomplicated understanding and smooth process.

Training slides are indispensable visual resources for supporting the content of any educational session, whether in seminars or as part of company training. They can be used to teach a new skill or simply increase knowledge on a given topic, widely used in face-to-face sessions and empowered by the increase of our online activity. Whatever the target audience and ultimate goal, we will help you develop engaging training slides tailored to the objectives of the presentation.

Slide decks are powerful visual aids aimed to communicate medical or scientific data in a more appealing and concise way. Whether for work presentations, conferences, or as training resources, they can target a wide audience, from experts to the general public. A well-crafted deck presentation should back up your words with a clear organisational design, helping the audience to better digest complex concepts and grasp a clear take home message. Let us help you create captivating, personalized presentations that ultimately yield impactful results.

Systematic reviews rigorously compile all available data on a specific topic, helping researchers understand the state-of-the-art and avoid unnecessary duplication of studies and resources. From a clear scientific question as a starting point, it is essential to create a systematic search protocol, carefully distil the outputs obtained, and finally analyse and interpret the results derived. We will help you identify if your question has already been answered, if there is a niche to exploit, or if it needs to be refined in order to move forward with your next steps.

Original articles are in-depth research reports intended to communicate new data and discoveries, pushing the boundaries of knowledge. Typically published in peer-reviewed journals, they can be nourished from a wide range of sources, from clinical trials to new laboratory findings. Complex scientific data should be presented in a clear, organised, yet engaging style in order to reach not only experts in the field but also those outside it. We will bridge that gap while adhering to the journal's guidelines, helping gain acceptance and facilitating a well-informed decision.

FAQs Archive - Page 4 of 5 - Azur Health Science

Q: Investigator Brochures (IBs)

The Investigator Brochure is a dynamic document, containing all clinical and non-clinical information about the investigational product. It serves as a guide to ensure that everyone involved in conducting the study has the most up to date knowledge to safely run the trial. To that end it is a document that is regularly updated over the course of the lifecycle of drug development The IB balances complex information with clear safety instructions that must be accessible to the entire team. That is why we specialise in distilling the content into an accurate and readable format to support the needs of researchers while ensuring patient safety.

Q: Clinical Study Protocol (CSP)

The Clinical Study Protocol is a critical document that describes what will be done in the study, how it will be done, and why it is being done. It is a roadmap for properly conducting a specific clinical trial, ensuring that objectives are met and participants’ safety is guaranteed. Therefore, the language must be clear and understandable by various stakeholders. We will bring our experience working with cross-functional teams to provide well-structured, scientifically sounded and regulatory compliant deliverables.

Q: Response to Media Questions

Media coverage of medical advances is essential these days, as most of the general public obtains their health information through them. Therefore, crystal-clear responses to media questions are pivotal in order to convey the right message, striking a balance between what is "new" and what is "important," so that the media can carefully assess the real significance of the medical information they receive. We will draft distinct and reasoned messages in line with our client's objectives, to ensure they resonate among the audience.

Q: How does Azur Health Science Mentoring work?

You can take a look at the learning options most suited to you, and decide whether you want to have hands-on experience in Medical Writing projects, for which you will receive constructive, personalised feedback or if you are just looking into the profession for more information. Either way, you will gain detailed insight into what medical writers do daily and learn how to hone your writing skills for your chosen career. The mentoring covers topics such as: • Industry culture and ethics • Working as part of a multi-function team • Writing style, readability and targeting your audience • Clinical development and the product life-cycle

Investigator Brochures (IBs)

Patient Information

Protocol Amendments

Clinical Study Protocol (CSP)

Training Slides

Response to Media Questions

Slide Decks

Systematic Reviews

Original Articles

How does Azur Health Science Mentoring work?

Training portal

Contact

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