The number and complexity of regulatory documents has increased significantly in the last decade as the volume of clinical trials and the regulatory burden have grown. The expedited clinical research for Covid -19 vaccines and therapeutics has further demonstrated the need for rapidly generating high quality regulatory documents to ensure patient safety [...]
Plain language summaries (PLSs) aim to meet a need in the industry for clinical trial transparency in a way that is meaningful and understandable for patients and the general public. As the pharmaceutical industry steps up to meet this requirement, patient panels play a crucial role in ensuring that information shared by sponsors [...]
Join this free webinar to learn how the pharmaceutical industry is engaging with patients and patient advocates to gain feedback and produce high-quality plain language summaries. When Friday December 06th 9 am EST | 2pm GMT | 3pm CET | Register
From 22nd-23rd February, Kinapse is sponsoring the ISCR's two day symposium on Medical Writing at the Central Drug Research Institute, in Lucknow, India.
Our best-practice webinar on EMA Policy 0070 compliance will feature first-hand accounts of some of the experiences and lessons learnt from 21 external submissions made by 9 pharma firms. Reserve your place On February 21st 2018, we're hosting a practical webinar illustrating how life sciences companies are managing clinical trial [...]
Our multinational forum makes 4 practical recommendations to help ensure the continued well-being of patients across the UK and EU27 following Brexit.
On Thursday 23rd November, we hosted the Kinapse Brexit Summit at the Royal Society in London. About the Summit The aim of the summit was to facilitate round table discussion and debate with key players from industry and patient groups on the subject of Brexit and its potential impact on these [...]