Boyds

Strategically leveraging regulatory designations can significantly impact the success of your drug development program. In our recent blog, Boyds' regulatory experts, Dr Julie Warner and Dr Katherine Bowen, demystify the intricacies of these regulatory designations, providing clarity on their strategic application and the potential complexities they can present. Read the blog here: https://lnkd.in/eWmaaAGx #RegulatoryDesignations #RegulatoryAffairs #FDA #MHRA #EMA #ODD #FTD #RMAT #BTD #PRIME #ILAP

Life Sciences businesses seeking funding and investment of £250k or more: The BioCap Pitching Competition is open until 6TH SEPTEMBER so get your applications in ASAP! Shortlisted applicants MUST also be available 24th (online) and 26th September (in-person) and will need to purchase a delegate ticket. Apply here: https://lnkd.in/etUkip64 💻 Send completed application forms to pitching.competition@bionow.co.uk with the subject line “2024 BioCap Pitching Competition”. #BioCap #Pitching #PitchingCompetition #LifeSciences #Funding Sponsors: Bruntwood SciTech | STFC | Mills & Reeve | RSM UK | Appleyard Lees IP LLP | Boyds

🚨 A new episode of Conversations in Drug Development is out now! In today's discussion, we are exploring the new EU Clinical Trials Regulation (CTR) and its significant impact on the regulatory environment. Our host Harriet Edwards is joined by Dr Katherine Bowen and Shalini Gupta to explore the transformative changes in the European Union's clinical trial landscape, focusing on the transition from the Clinical Trials Directive (CTD) to the Clinical Trials Regulation (CTR). Join us for an insightful discussion on how the CTR is shaping the future of clinical research in Europe and the positive impact it aims to have on patients. Tune in by searching "Conversations in Drug Development" on all streaming platforms or visit https://lnkd.in/e5Kk9iky #ConversationsinDrugDevelopment #Podcast #DrugDevelopment #CTR #CTD

There's still time to sign up for our free webinar where our experts, Dr Karen Mullen and Dr Harriet Gray Stephens share their tips and expertise on de-risking your clinical development plan. 📅 June 27th at 9am Pacific To register, visit https://lnkd.in/e8P2hwAt

The August edition of Boyds Regulatory Intelligence Digest is out now! This time we are bringing you all the latest guidance and key updates from the regulatory agencies - #FDA, #EMA, #MHRA, #IMDRF, and #WHO. 📧 To discuss any of these updates, please contact a member of the Boyds Regulatory team at info@boydconsultants.com who will be happy to help.

Meet Boyds in person near you! Boyds will be attending several conferences between September 11th and October 4th. If you're attending any of these conferences, Boyds welcomes the opportunity to meet and discuss your needs for regulatory, product development, program management, and clinical and medical support. See more details in the event post!

Maximise your networking opportunities at BioCap with a combined Delegate Pass & Investor Mixer ticket: Build connections on 25th September ahead of the conference then enjoy an agenda of panel discussions, keynotes and 1-2-1s the next day! https://lnkd.in/eXCvhVs4 #BioCap #Investment #Funding #Networking #LifeSciences Investor Mixer venue: THE ALAN BioCap venue: King's House Conference Centre Sponsors: Bruntwood SciTech | STFC | Mills & Reeve | RSM UK | Appleyard Lees IP LLP | Boyds

We recently welcomed fifth year medical student Sam Mayhew to Boyds on a work experience placement. In this guest blog, Sam describes his background, his research project at Boyds, and what he gained from the experience. Read his blog here: https://lnkd.in/ewhi_RQm #workexperience #placement #drugdevelopment

Boyds' medical writing experts have years of authoring experience and are highly skilled in preparing well-written, scientifically accurate and polished documents that meet all regulatory requirements. For high-quality, flexible support with your clinical and regulatory documents, get in touch with one of our experts today. To find out more, visit https://lnkd.in/e_ZACNZ5

Boyds team of regulatory operations and publishing experts optimizes and streamlines the submission process, ensuring your submissions are accurate, compliant and on time. As a global company, with offices in the US, UK and Europe, the team at Boyds can support clients with submissions to FDA, MHRA and EMA, and can provide US Agent support, when required, to interact with the FDA on our client’s behalf. For more information, visit https://lnkd.in/eeahR2Qx #eCTD #RegulatoryCompliance #RegulatoryOperations