Meet the Medics
In this new interview series, we sit down and meet the medics at Boyds to find out about their career backgrounds, their interest and passion for medicine, their greatest achievement – whether personal or professional – and get their insights on the latest industry trends.
Boyds collaborates with BioPharma Connections
![Biopharma connections](https://boydconsultants.com/wp-content/uploads/2024/01/Website-news-cover-image-size-63.png)
Boyds partners with BioPharma Connections in the company’s latest move to continue its growth in the U.S.
Double win for Boyds at TOPRA Awards 2023
![TOPRA Awards 2023](https://boydconsultants.com/wp-content/uploads/2023/11/d9f97b54-8f63-43eb-a96b-036940ec0392-1024x742.webp)
The TOPRA Awards 2023 saw the Boyds team take home two awards, with our regulatory affairs team crowned winners of the Futures Award and our Senior Director of Regulatory Affairs Katherine Bowen awarded the Inspiration Award. The TOPRA Awards for Regulatory Excellence are the annual international awards for celebrating achievement and best practice in regulatory […]
Boyds grows regulatory affairs team with new hire
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We are delighted to announce the appointment of Monica Pianella as Associate Director of Regulatory Affairs. With over seven years’ experience in advanced therapies, Monica joins Boyds from the Cell and Gene Therapy Catapult (CGTC) where she was Senior Regulatory Affairs Manager working in early drug development with a strong focus on CMC and cell […]
Boyds launches ‘Conversations in Drug Development’ podcast
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Boyds has announced the launch of a brand-new podcast series that aims to keep the scientific and clinical community abreast of the latest advancements in cell and gene therapy and drug development.
Chris Moore discusses key considerations for US biotechs setting up gene therapy studies in Europe
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In the viewpoint article: ‘Key considerations for US biotechs setting up gene therapy studies in the UK and Europe’, Chris highlights some of the important things organisations must consider before initiating their study.
Regulatory Submissions
![Conversations in Drug Development](https://boydconsultants.com/wp-content/uploads/2023/10/Website-news-cover-image-size-53.png)
Welcome to Conversations in Drug Development, brought to you by the team at Boyds. This podcast is for our fellow community of scientists and clinicians working in the wonderful world of cell and gene therapy and drug development.
The UK Innovative Devices Access Pathway (IDAP) pilot scheme now open for application
![The Innovative Devices Access Pathway](https://boydconsultants.com/wp-content/uploads/2023/10/Website-news-cover-image-size-58.png)
![The Innovative Devices Access Pathway](https://boydconsultants.com/wp-content/uploads/2023/10/Website-news-cover-image-size-58.png)
The UK has launched The Innovative Devices Access Pathway (IDAP) pilot, a new pathway to support the rapid development of innovative technologies.
Experts at Boyds share ten top tips for starting an early phase clinical trial
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![](https://boydconsultants.com/wp-content/uploads/2023/10/Website-news-cover-image-size-56.png)
The clinical operations and medical affairs experts at Boyds have shared their ten top tips for how to start and promote the success of early phase clinical trials.
Podcast | Conversations in Drug Development
![Conversations in Drug Development](https://boydconsultants.com/wp-content/uploads/2023/10/Website-news-cover-image-size-53.png)
![Conversations in Drug Development](https://boydconsultants.com/wp-content/uploads/2023/10/Website-news-cover-image-size-53.png)
![Conversations in Drug Development](https://boydconsultants.com/wp-content/uploads/2023/10/Website-news-cover-image-size-53.png)
Welcome to Conversations in Drug Development, brought to you by the team at Boyds. This podcast is for our fellow community of scientists and clinicians working in the wonderful world of cell and gene therapy and drug development.