Global medtech News

Starting in a new job always involves anxiety, expectations and the natural learning curve. But when this experience happens on another continent - with another work culture - the impact can be even greater. If you come from the Brazilian market and are joining the European industry, it is important to understand that the onboarding process (integration and monitoring of the new employee) works differently. Below, we highlight the main points of contrast: 1. Structure and formalisation of onboarding Brazil: Onboarding can vary greatly between companies. In many organisations, there is an initial focus on administrative aspects (documents, access to systems) and a presentation of the culture and area. However, there is not always a structured continuous monitoring program. Europe: In most European countries, especially in multinational companies, onboarding is highly structured and follows a clear integration plan, which can last from 30 to 90 days or more. The process usually includes:...

The transition from the hospital environment to the universe of medical writing may seem challenging, but it is totally possible - and very strategic! The pharmacist already carries a valuable technical background that can be applied directly in the scientific and regulatory writing, especially for his practical experience with medicines, protocols and clinical data. Steps to become a Medical Writer: 1. Understand what a Medical Writer does Medical writers transform technical information from the health area into clear, objective and well-structured content. This can include everything from scientific articles to regulatory documents and educational materials. 2. Take advantage of your clinical background You already have in-depth knowledge about medicines, pharmacology, clinical protocols and even pharmacovigilance. All this is gold in medical writing. 3. Invest in specific training Search for courses on: •Scientific writing •Regulatory writing •Pharmacovigilance •Clinical research (G...

If you dream of migrating to areas such as Regulatory Affairs, Medical Devices or Pharmacovigilance, but feel that the budget is short, know that it is possible to specialise with intelligence, focus and few resources. I have been walking this path myself - and I can say: it works! Here is a practical guide for those who want to learn consistently and spending little: 1. Start with a clear goal and a learning trail Choose an area (e.g. Regulatory Affairs, QA, Clinical Trials) and set up a study trail with the main themes. You can organise this in a planner, notebook, spreadsheet or app like Notion, Trello or even Google Keep. The important thing is to have a clear vision of what to study and where to start. 2. Use accessible (or free) platforms Here are some great options: • Coursera, edX: free courses from renowned universities (with paid certificate option). •FutureLearn: courses on medical devices, regulation and public health. •OpenWHO: great content on pharmacovigilance, healt...

If you write frequently - whether technical, scientific, creative or professional texts - it is likely that you have already looked for ways to improve clarity, fluidity and impact. And that's exactly what Gary Provost delivers in 100 Ways to Improve Your Writing. What makes this book special? Unlike theoretical manuals, this book is objective, practical and straight to the point. With short chapters, it offers applicable tips from the first paragraph. No generic rules: each of the "100 ways" is explained with examples and context. Some of the topics covered include: •How to make your writing clearer and more engaging •The importance of rhythm and variation of sentences •Tips for reviewing and cutting excesses •How to keep the reader interested until the end •The difference between writing to sound intelligent and writing to be understood One of the most striking excerpts: "This sentence has five words. Here are five more words. Five-word sentences are fine. But seve...

If you are a pharmacist or health professional and want to migrate to the area of Medical Writing, but don't know where to start, this post is for you! We have prepared a 4-week study plan to guide you through the fundamentals of scientific writing and present the universe of Medical Writing. Let’s start with me? Week 1 to 4 - Introduction to Medical Writing and Scientific Language Objective : Understand what Medical Writing is, its different types and the basic principles of clear, objective and evidence-based scientific writing. ⸻ What is Medical Writing? Medical Writing is the production of technical and scientific content on health, medicines, clinical studies and health education. The performance can vary from the creation of regulatory documents to educational materials for patients. Main Types of Medical Writing: • Regulatory writing - documentation for agencies such as ANVISA, FDA, EMA; • Scientific publications - scientific articles, reviews, clinical studies; • Medical ...

Inventory control is one of the most sensitive and strategic gears in the pharmaceutical area, whether in the hospital or industrial environment. Effective management avoids waste, ensures patient safety and maintains regulatory compliance. Although the contexts are different, both require organisation, continuous monitoring and data-driven decisions. Next, see specific strategies for each scenario: ⸻ In hospital pharmacy: focus on agility and patient safety In the hospital, the stock is directly linked to care. Any failure can compromise the treatment. How to optimise: 1.ABC x Criticality Rating •Organise medications by volume of use (ABC) and clinical criticality. This helps to prioritise the replacement of essential inputs. 2. Replacement point and minimum stock •Establish safe inventory levels, based on replacement time, average demand and disruption risks. 3.Regular inventories •Perform periodic counts (cyclical and general) to identify losses, malfunctions or deviations. 4.In...