Hosted by Olga Peycheva
Episodes
54
Latest episode
Jun 2026
Language
EN
This podcast is dedicated to clinical trials and clinical research. We will be discussing different hot topics and analysis of the latest developments in clinical trials in pharmaceutical and medical devices industries. We have interviews with different industry experts. New episodes will be available every 2 weeks.
Clinical trials GCP inspections are common but the expectations can vary between different inspectors and agencies. In this episode, we are discussing with my colleague Lydia Ainsworth, what we learnt during the GCP inspections that we had in Europe in 2025. We cover some key inspection preparation points for the sponsors but also for the hospitals.
This episode is a follow up on round table discussions during the ICR Conference on 13 and 14th of April 2026 in Birmingham. We discuss the common issues related to setting up clinical trials in the UK and also the challenges with adaptation of electronic site files and digital technologies in clinical research. We also provide some recommendations how the processes can be improved and streamlined.
In this episode we discuss with Lydia Ainsworth, our Senior Clinical Data Quality Manager, what we learnt from the Institute of Clinical Research (ICR) Conference, 13-14 Apr 2026.The conference covered the latest clinical trials regulatory changes which affect the pharma and biotech industry. There were representatives from UK regulators MHRA and HRA, but also from the industry, academia and NHS.You can learn about the clinical trials regulations changes; what is coming in the medical devices' field; the importance of patient engagement; the use of AI in clinical research; latest trends in drug development and other topics.You can read the transcript of the interview here: https://solutionsop.co.uk/2026/05/15/icr-conference-april-2026-the-latest-on-the-uk-clinical-trials-regulatory-changes/
This is a short overview of the current development of cell and gene therapies and their challenges. It discusses the different types of cell therapies; latest developments and the challenges of creating allogenic cell therapies. Terminology is avoided on purpose to present the information in accessible way for those without scientific background.
In this episode we decided to use a new approach in regulatory affairs and tell people how to fail their BLA (Biologics License Application) and piss off their FDA reviewers at the same time. In order to do that, Arvilla Trag, who is a Chemistry, Manufacturing and Controls (CMC) industry expert helped by walking us through the FDA CMC Hell where we met all kind of people from pharma companies and heard all kind of interesting ideas on how not to complete the CMC section.We would like to apologize to anyone who accidently learnt something from our entertaining discussion!You can read the transcript of our discussion here: https://solutionsop.co.uk/2026/04/17/visiting-the-9-circles-of-fda-cmc-hell-with-arvilla-trag/
In this episode we are discussing the clinical research opportunities in Japan. Our guest is Tetsu Yung who is a consultant with extensive experience in pharma and CRO industry in Japan. We cover the main requirements for setting up clinical trials in Japan and the timelines for obtaining approvals. We also talk about initiatives from the Japanese government to encourage pharma start-ups to set up in Japan and conduct their clinical research in the country.You can find the script for the interview here: https://solutionsop.co.uk/2026/04/10/clinical-research-opportunities-in-japan-interview-with-tetsu-yung/
In this episode we are talking with our Senior Clinical Data Quality Manager, Lydia Ainsworth, about animal testing in clinical research.Join us to learn:What are the most common animals used in animal testing,The typical cost for using animals in clinical research,The ethical issues around using animals,When animal testing is needed in drug developmentWhat are the alternatives of animal testing.You can find transcript on our discussion here: https://solutionsop.co.uk/2026/03/25/do-we-need-animal-testing-overview-with-lydia-ainsworth/
This episode is an analysis of the latest investment trends in research and development in the pharma industry in 2026. You can learn what has changed in clinical research and the way companies invest in developing new drug products. It touches on investment risks, price pressure and the threat from biosimilars.
In this episode of the podcast, we discuss with Richard Vincins, medical device expert from MD Compliance, the medical device registration process in Europe and the challenges that the small and mid size manufacturers face. We also discuss what could be done to help medical device manufacturers to improve market access and innovations in Europe.You can find the transcript of this episode here: https://solutionsop.co.uk/2026/03/02/medical-devices-registration-in-europe-interview-with-richard-vincins/
In this episode we talk about clinical trials in primary care and the role of general practitioners (GPs) and family doctors in clinical research with the Dr Daphne Hazell who is a GP and CEO of the biggest GP network in the UK which is involved in clinical research. We discuss the challenges and the benefits of using primary care in clinical research.You can read our transcript to the interview here: https://solutionsop.co.uk/2026/02/09/the-role-of-family-doctors-in-clinical-research-interview-with-daphne-hazell/
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The National Academy of Sciences
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