Due to our extensive experience in pharmacovigilance, both national and international (European Medicines Agency), you can expect us to have an answer to all your pharmacovigilance questions. We can help you to comply with authorities’ regulations. We advise on risk management plans, post-authorisation studies, real world evidence and SmPC or leaflet wordings. You can depend on us for all pharmacovigilance questions you have: whether that will be in a pre-licensing, application, or a post-authorisation situation. We are specialised in vaccines, orphan medication, and anti-hiv-medication.
Apart from being expert in all pharmacovigilance issues regarding all kinds of vaccines, we have extensive expertise and knowledge on most aspects of vaccination. We are happy to discuss and analyse public health issues, new developments, new vaccines and techniques. Next to that, we have international vaccination expertise, for instance on procurement, and public health issues.
If you need someone to thoroughly read and comment your medical thesis, research paper or any other medical (scientific) text in English or Dutch, we can help you. If you should want to skip a lot of words in your publication, we can easily reduce the numbers of words and even make your text better. With our many years of (peer) reviewing and medical writing we make your text accurate and succinct. Also in Dutch!
