Insights
Our specialist team here at JensonR+ is experienced in regulatory affairs, product development, quality assurance, drug safety, medical information, copy approval, project management, training and market access.
Here we share insights into our ways of thinking in this changing landscape. Any questions please talk to us, we are happy to start the conversation.
Pharmacovigilance Auditing and Training
We’ve expanded the team of our experts that are trained and experienced in conducting audits and mock inspections that meet all of your PV needs.
Congratulations Shane
Congratulations to Shane Sankey on 10 years’ service at JensonR+
EMA and PIC/s Issue Concept Paper for GMP Annex 11 (Computer Systems)
A 5-page concept paper was issued by the European Medicines Association (EMA) and Pharmaceutical Inspection Co-operation Scheme (PIC/s) on 16th November 2022 with a deadline for comments by 16th January 2023.
A career in pharma
How did some of our team find their way to working at JensonR+ and how do they feel about their chosen career? We've been asking the questions and to kick things off, let's hear from Karen Bradshaw in our Regulatory team.
Women’s Health – A Holistic Approach – Review
World Menopause Day saw JensonR+ partnered with Medilink Midlands for our Food Supplements Special Interest Group. This in-person event was dedicated to how nutrition and supplementation can impact women’s health.
Another happy Jenson client
We pride ourselves on being responsive to our clients and incorporate feedback into our activities. Nobody can tell you about our services better than our clients, so we’re happy to share some recent feedback that we received following a project that one of our RPs Chloe Child worked on.
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