We're #hiring a new Customer Service Specialist in Mumbai, Maharashtra. Apply today or share this post with your network.
DIA
Pharmaceutical Manufacturing
Washington, DC 37,997 followers
Driving collaboration in drug, device, and diagnostics development in pursuit of a healthier world
About us
DIA is the leading global life science membership association driving collaboration in drug, device, and diagnostics development in pursuit of a healthier world. Founded in 1964 with headquarters in Washington, D.C., and offices in Europe and Asia, DIA provides unparalleled networking opportunities, educational resources, scientific research publications, and professional development programs to members in more than 80 countries.
- Website
-
http://www.DIAglobal.org
External link for DIA
- Industry
- Pharmaceutical Manufacturing
- Company size
- 51-200 employees
- Headquarters
- Washington, DC
- Type
- Nonprofit
- Founded
- 1964
- Specialties
- Professional Association, Pharmaceuticals, Medical Devices, Biotechnology, Education Provider, Government, Clinical Trials, Education, Training, eLearning, Translational Medicine, Patient Engagement, Value and Access, healthcare, regulatory affairs, Pharmaco Vigilance, personaldevelopment, careers, women in science, and medicine
Locations
Employees at DIA
-
Eli Weinberg, PhD
Developing and delivering innovations in medicine
-
Joe Dustin
VP, Product Strategy | BioFourmis | eClinical Tech Executive | Advisor | AI | eCOA | DHTs | Decentralized Trials | Clinical Operations
-
Timothy Hess
Global Head of Business & Digital Technology at DIA
-
Nimita Limaye
Research VP, Life Sciences R&D Strategy and Technology, at IDC
Updates
-
We're excited to partner with Regulatory Affairs Professionals Society (RAPS) again this January for the 2025 Combination Products in the EU. It'll be another highly interactive event that will unite key stakeholders across the field — including representatives from EMA, the European Commission, Notified Bodies, National Competent Authorities and Industry — to explore a coordinated drug and device approach to incentivize competitive innovation in Europe. Make plans today to engage with experts and exchange ideas that stimulate ideation and innovation to drive solutions 28-29 January 2025 at the Radisson Grand Place in Brussels, Belgium. Plus, register by 06 December 2024 for the early-bird discount: https://bit.ly/3YipPQi.
-
We're #hiring a new Senior Accountant, EMEA in Basel, Basel. Apply today or share this post with your network.
-
𝐅𝐢𝐧𝐚𝐥 𝐑𝐞𝐦𝐢𝐧𝐝𝐞𝐫: Call for Professional Posters for DIA Europe 2025 closes on 16 October. This is your last opportunity to submit your research and present it to a diverse group of experts in pharmaceuticals, biotechnology, and healthcare. Submitting a poster allows you to gain valuable feedback, network with professionals across the drug development continuum, and share your specialised research with a broad, interdisciplinary audience. Submit your poster today: https://bit.ly/3Ym9Mkz. #DIAEurope2025 #CallForPosters #Posters
-
Mark Your Calendars! Upcoming DIA Events You Don’t Want to Miss! 🗓️ Whether you're a healthcare professional, regulatory expert, or industry leader, DIA events provide the perfect platform to stay ahead in the world of life sciences. Real-World Evidence → October 24-25th, 2024 | Philadelphia, PA https://ow.ly/CXq650TJLP3 Oligonucleotide-based Therapeutics → October 28-30th, 2024 | Washington, DC https://ow.ly/XVga50TJLSY DIA Direct Webinar: Driving Adoption and Value Across the Regulatory Information Management (RIM) Ecosystem → November 13th, 2024 | 11:30-12:30PM https://ow.ly/kEut50TJLEF Canada Annual Meeting → November 14-15th, 2024 | Gatineau, QC, CA https://ow.ly/mqJK50TJLUE DIA Webinar: Inclusivity as a Part of Feasibility : Making Trials More Representative with RWD→ November 19th, 2024 | 12:00 PM https://ow.ly/jYSy50TJM39 Solution Provider Webinar: Polaris by OM1: Clinical Trial Recruitment for Faster, Cost-Effective Trials → November 19th, 2024 | 2:00-3:00PM https://ow.ly/4PrM50TJMk9 Global Pharmacovigilance and Risk Management Strategies Conference → January 27-29th, 2025 | Baltimore, MD https://ow.ly/Movn50TJLXE
-
+2
-
DIA reposted this
👀 Featured Event: DIA's Real World Evidence Conference 👀 📆 24 October 📍 Philadelphia, PA, USA. As RWE takes its rise within the industry, with its ever increasing role within he product development lifecycle, and has led to the real-time analysis of data to better understand and gain insights on disease, approaches to treatment, and how to substantiate coverage decisions. It is important we ensure we stay ahead of the trend. Join DIA in Philadelphia this October at their Real World Evidence conference where they will explore new, innovative applications of RWE, and deliver cutting-edge insights to leverage this knowledge to advance healthcare decision-making. Keen to hear from the experts in the field, join the following speakers: David Martin, Jaclyn Bosco, John Concato, Diane Gubernot, Dr. Rachele Hendricks-Sturrup, Camille J., Charles Lee, Sarah K. Martin, MS, PhD, Brittany Avin McKelvey, Keri Monda, Tamei Elliott, Antonia Electra Panayi, Tim Wolfe, Kelly Magee, Gary Male, Troy Astorino, Mike D'Ambrosio, Lisa Ensign, Gabriel K. Innes,Mehdi NajafZadeh, Dan Riskin. Delphine Saragoussi, MD, MScPH,Lina Titievsky, Jenna Wong, Jonathan Assayag, Melinda Baker, Ulka Campbell, Sarah Dutcher, Sarah Ferko, PMP®, Christian Hampp, Jingyu (Julia) Luan, PhD, RAC, Susant Mallick, David Pritchard, James Browning, Jeffrey Brown Nuvan Rathnayaka, Flavio Dormont, PhD, MBA, Claudia A Salinas, as they share their invaluable insights! Set to be the RWE event of the year - don't miss out! Find out more at MyMA: https://lnkd.in/eK3tFVQH #RWE #pharma #conference #RWD #DIA Kara Brown - MPS-IMC, PMP®
-
Join us for the ‘Introduction to the Role of QPPVs’ tutorial, taking place prior to the Global Forum for Qualified Persons for Pharmacovigilance (QPPV) in Amsterdam. This workshop is tailored for QPPVs, those who support them, and anyone considering this critical role. It will cover responsibilities, implementation across various company structures, business partner management, quality oversight, and legal considerations. Elspeth McIntosh and Magnus Ysander have recorded a video offering a sneak peek into the tutorial, discussing its highlights and benefits. Tune in to discover how this workshop can enhance your understanding of the QPPV role and expand your professional skill set. Secure your spot today: https://bit.ly/400Lmht. #Pharmacovigilance #Workshop #DrugSafety #QPPV
-
FREE WEBINAR: Optimising Lifecycle Management in the Middle East and North Africa (MENA) Join us for an exclusive live virtual webinar on 29 October at 10:30 CET, as we explore opportunities to optimise lifecycle management of medicinal products in the MENA region by expanding the use of Reliance to Post-Approval Changes (PACs). This session will feature industry experts discussing how to enhance regulatory approval processes, address CMC and labelling complexities, and ensure a continuous supply of critical medicines. Don’t miss this key opportunity for professionals in the pharmaceutical industry, regulatory bodies, and academia! Secure your spot here: https://bit.ly/4eYdXbw. #DIAMENA2024 #Webinar #RegulatoryAffairs #Reliance #PACs
This content isn’t available here
Access this content and more in the LinkedIn app
-
The #RegulatoryPolicyForum is for regulatory policy leaders, senior decision makers, and regulators across the pharmaceutical community. DIA and Regulatory Affairs Professionals Society (RAPS) have partnered once again to highlight the new EU pharmaceutical legislation and how it will shape the future of the pharmaceutical arena — including research, development and manufacturing — in Europe for decades to come. The agenda is curated by experts across the pharmaceutical community to ensure you'll participate in the highest quality discussions, knowledge exchange, and collaboration opportunities. NOTE: Early-bird pricing ends October 18. This is an event all regulatory leaders should have on their schedules. Save your seat today: https://bit.ly/3YMFisn.