Why I chose to join Kinapse Catherine Egles, Sales Operations Associate, recalls how she came to join Kinapse and why she's happy she chose to come work with us. During my time at The University of Reading studying Biomedical Sciences, the two most popular routes post-graduation were to go into research [...]
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So far Rich Jinks has created 8 blog entries.
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 [...]
After months of speculation, the EMA has been committed to take up operations at a site in Amsterdam by 30th March 2019. The decision was reached by vote from the EU 27 Member States. How should your organisation prepare? A decision has been made – and that is good [...]
Why I chose to join Kinapse Having joined Kinapse in October, Adam Sherlock shares the reasons he chose us, and his hopes for the future of the business. I’ve been in life sciences my whole career – 30 years this year – and I’ve been on the service provider side and [...]
New appointment drives global service delivery Hemant Manohar has been appointed as Head of Global Service Delivery (GSD), based in India. This new senior appointment is part of Kinapse’s strategy to expand its global delivery model to support clients on a worldwide scale. Hemant has a wealth of experience in Life Science [...]
AI - Is the Life Sciences industry playing catch-up? John Cogan, Head of Innovation, shares his views on what R&D functions should be focusing on to maximise Artificial Intelligence opportunities. After reading with interest a recent Times article outlining the role that robots are playing in helping transform the healthcare sector, it’s clear that [...]
The current industry outlook on Plain Language Summaries Following her panel discussion at the recent CBI Lay Summaries Conference in Philadelphia, Pooja Phogat, VP and Clinical Trial Disclosure Technical lead, shares some of the recommendations discussed at the conference. Attended by representatives from various global pharmaceutical companies, the CBI Lay Summaries Conference [...]
Easing the EMA Policy 0070 burden with the launch of redact360 Our clients are finding that complying with the new EMA Policy 0070 regulation is time consuming and costly, and precious staff time is being taken up with manual redaction processes and efficiencies lowered as they fail to standardize their processes. Pooja Phogat, [...]