
In this episode we are discussing with Harry Henson, the associate director of RBW Consulting, how AI will reshape the healthcare and pharma industry. Is AI making the recruitment process more efficient? Would AI make...


health
Hosted by Olga Peycheva · health · 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.
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Contact path
Verified email
Booking probability
33%
Guest openness
Selective
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Signup to Generate a PitchThis 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.
Solutions OP Clinical Trials UK is hosted by Olga Peycheva. The show has published 63 episodes to date.
Recent episodes include "How Will AI Reshape the Recruitment in Healthcare: Interview with Harry Henson" (30 October 2026, 26 minutes), "What Caused The Global Crisis of Antibiotics Resistance" (16 October 2026, 31 minutes), and "Do We Need Women Participants in Clinical Investigations for Medical Devices" (2 October 2026, 24 minutes).
Solutions OP Clinical Trials UK publishes roughly every two weeks, with episodes averaging 29 minutes across 63 episodes.
Booking probability for Solutions OP Clinical Trials UK is 33%, and the host is rated Selective on guests. Solutions OP Clinical Trials UK requires a Pod Score of 80 or higher. Solutions OP Clinical Trials UK's contact route on record: verified email.
The strongest fits for Solutions OP Clinical Trials UK are Scientific Research & Development. Solutions OP Clinical Trials UK has a health audience.
Olga Peycheva hosts Solutions OP Clinical Trials UK, a health podcast with 63 episodes published.
Our AI reads these to draft pitches. Use them as grounding for a pitch that cites a real guest and a specific topic.

In this episode we are discussing with Harry Henson, the associate director of RBW Consulting, how AI will reshape the healthcare and pharma industry. Is AI making the recruitment process more efficient? Would AI make...

In this episode we discuss with Lydia Ainsworth the global antibiotics crisis and the reasons for this crisis. In addition, we mention some of the drug development trends and some ideas how to encourage antibiotics...

In this episode we review why we need women to participate in clinical research with medical devices. We also cover the FDA guidance on sex-specific data collection for medical devices and its main recommendations on...

This episode is a review of a white paper from Aug 2026 on dose optimisation for radiotherapeutics. In addition, Lydia Ainsworth reviews the FDA guidance covering the same topic and providing FDA recommendations. The...

In this episode we review with Lydia Ainsworth an article discussing ethical challenges for clinical research with implantable neural devices. The overview provides valuable insights for ethics committees, researchers...

This episode is dedicated to psychedelics research. It covers the recommendations from the US FDA guidance from Jul 2026 which clarifies the agency's expectations regarding the drug development and clinical trials...

This episode covers the upcoming changes in the clinical trial regulations in Canada based on information presented by Health Canada. It also contains global trends analysis and comparison to the regulatory changes in...

This episode is an overview and analysis of the discussions from the 3rd day of the 5th FDA, MHRA and Health Canada Symposium in June 2026. It covers international initiatives for harmonisation of drug safety review...

Our latest podcast is dedicated to bioequivalence studies and their specific challenges. We also cover what was discussed in terms of inspection findings, cases studies and expectations by FDA and Health Canada on their...

This episode is review and analysis on the first day of the 5th FDA, MHRA and Health Canada Symposium in June 2026 which covered GCP, clinical trials and risk management.

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...

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...

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...

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...

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...

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...

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...

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...

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...

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...
Recent guests on Solutions OP Clinical Trials UK. Study who booked and why before you pitch.
chair of Fulham Ethics Committee, pRx Engage
President and CEO, TARGEGEN Pharmaceuticals
MD Compliance
Royal Marsden Hospital
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