The July issue of our #GlobalForum is now live! This month, we're diving into groundbreaking topics shaping the future of #global healthcare and #clinical trials with articles like these: 💡#ClinicalTrials in Wartime: One Patient’s Journey to Survival 💡Implementing #Patient-Reported Outcomes in #Cancer Clinical Trials 💡How to Communicate Unapproved Uses Without Breaking the Law Stay informed. Stay connected. Together, we're advancing the field! https://ow.ly/PCqT50SzUKw #HealthcareInnovation #DataTransparency #GlobalHealth
DIA
Pharmaceutical Manufacturing
Washington, DC 36,992 followers
Empower healthcare innovation with DIA
About us
Experience the power of collaborative innovation with DIA (Drug Information Association)!Since 1964, our passionate, volunteer-based global network works together to provide strategic clarity, direction, and policy objectives to offer all stakeholders opportunities to co-create, problem-solve, and illuminate cohesive pathways to the future of global and regional life sciences developments. Join our dynamic, nonprofit organization that serves as a hub for life sciences professionals, academia, advocates, and policymakers worldwide. At DIA, we foster interdisciplinary connections, engaging patients, peers, and visionary leaders in tackling today's challenges and shaping tomorrow's breakthroughs. Unleash your potential with our knowledge resources, cutting-edge conferences, and transformative training courses. From product development to regulatory science and therapeutic innovation, we provide the tools and insights you need to excel. With our headquarters in Washington, DC, and regional offices spanning the Americas, Europe, Africa, the Middle East, and Asia, we're strategically positioned to drive change on a global scale. Let's revolutionize the future of healthcare together! To learn more about our mission, visit DIAglobal.org or connect with us on Twitter, LinkedIn, Facebook, and Instagram.
- Website
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http://www.DIAglobal.org
External link for DIA
- Industry
- Pharmaceutical Manufacturing
- Company size
- 51-200 employees
- Headquarters
- Washington, DC
- Type
- Nonprofit
- 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
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Eli Weinberg, PhD
Developing and delivering innovations in medicine
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Joe Dustin
VP, Product Strategy | BioFourmis | eClinical Tech Executive | Advisor | AI | eCOA | DHTs | Decentralized Trials | Clinical Operations
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Timothy Hess
Global Head of Business & Digital Technology at DIA
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Nimita Limaye
Research VP, Life Sciences R&D Strategy and Technology, at IDC
Updates
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The EU regulatory landscape for medicine development is complex, but our session from DIA Europe 2024 on ‘Complexity: Interplay and Interface of Different Legislations’ can help! This session explores the challenges and opportunities that arise when various regulations intersect in the development and manufacturing of medicines. Join a diverse panel of experts including medicine developers, policymakers, regulators, patients, and academics as they discuss: ◾ The impact of overlapping regulations in R&D and manufacturing. ◾ Practical strategies to navigate these complexities. ◾ Guiding principles for effective policy development. Don't miss this valuable resource! Watch the session now and gain insights to navigate the evolving regulatory environment: https://bit.ly/46iCK7n. For more information and to stay updated on DIA Europe 2025, visit our website: https://bit.ly/3LmbH19. #DIAEurope #HealthcarePolicy #Learning #RegulatoryAffairs
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{𝐍𝐞𝐰 𝐞𝐁𝐨𝐨𝐤 𝐉𝐮𝐬𝐭 𝐑𝐞𝐥𝐞𝐚𝐬𝐞𝐝!} 𝐀𝐜𝐡𝐢𝐞𝐯𝐢𝐧𝐠 𝐄𝐱𝐜𝐞𝐥𝐥𝐞𝐧𝐜𝐞 𝐢𝐧 #𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐈𝐧𝐟𝐨𝐫𝐦𝐚𝐭𝐢𝐨𝐧 𝐌𝐚𝐧𝐚𝐠𝐞𝐦𝐞𝐧𝐭 Get our eBook and learn valuable insights for #RegulatoryDrug teams: Best Practices in #RIM Capabilities and Functional Interfaces: https://ow.ly/e5mX50SzRO7
DIA eBooks: Achieving Excellence in Regulatory Information Management
diaglobal.org
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Don't miss BioSpace's Lori Ellis (Katz) in her incredible interview with FDA's Dr. Peter Marks!
At the DIA Global 2024 Conference, Dr. Peter Marks, Director of the Center for Biological Evaluation and Research (CBER) at the FDA, and Lori Ellis (Katz), Head of Insights at BioSpace, discussed the advancements being made to help drive forward drug and medical device development. Watch the full interview: https://lnkd.in/ga_z9spj #pharma #policy #biospace
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Ready to increase your expertise in risk management plans? Join our exclusive live-virtual training course this September and explore the essential aspects of creating an EU Risk Management Plan (EU-RMP). Here’s what you will gain: ◾ Hands-on experience in project management, medical writing, and maintenance of EU-RMPs. ◾ A thorough understanding of GVP Module V (Rev. 2) and its impact on Marketing Authorisation Holders. ◾ An advanced preview of the upcoming changes in the GVP Rev 3 and RMP Template Rev 3, with a special emphasis on ATMPs. Don't miss out on this great opportunity to increase your expertise on RMPs with our expert instructors! Register by 30 July for the early bird rate: https://bit.ly/4bDrOlF. #RMP24 #Pharmacovigilance #DrugSafety #RMP #GVP
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On 4-7 November, join us at the Paediatric Investigation Plans course. This training is a great opportunity to get a full introduction to the Paediatric Investigation Plans (PIPs) as well as the EU Paediatric Regulation. Curious about what you will learn? Hosted by leading experts from the EMA and consultancy, this course will cover: ✅ Definitions, Regulation, Guidelines ✅ PIP Lifecycle: Preparation, submission, modifications ✅ Global Paediatric Plan ✅ PIP Opinion ✅ Special issues: Pharmaceutical forms and formulations, non-clinical studies, clinical studies Register by 9 September to benefit from the early bird rate: https://bit.ly/4bzQSKd. Roberto De Lisa Mette Due Theilade Thomsen #PIP24 #PIP #PDCO #PaediatricInvestigationPlans
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Stay ahead of the curve and ensure successful submissions and reviews with DIA's comprehensive training on INDs, NDAs, and regulatory strategy. Join us today to elevate your regulatory knowledge and expertise! Learn More: https://lnkd.in/eX3tVeEy #NDA #FDA #Regaffairs #RegulatoryAffairs #lifescience
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Participating in DIA’s #tolerability research project offers many benefits, including first access to research findings and insights that can inform clinical trial design, treatment decisions, and benefit-risk assessments to gain regulatory approvals for cancer treatments. By joining, your organization will have the opportunity to define the future of tolerability in cancer treatment and enhance your visibility as a thought leader in the #lifesciences community. Discover the full range of partner benefits by emailing Radha.Goolabsingh@diaglobal.org. #Healthcare #Pharma
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Have you checked out the Solution Providers Marketplace yet? Discover the solutions you need, or offer your expertise to help organizations like yours thrive: https://ow.ly/E1Fs50SuHpz
Elevate Your #Business Growth with a Year-Round DIA #Marketplace Listing! Unlock the power of an annual #subscription to highlight your unique value proposition and be the go-to partner in the life science field. Don't miss this opportunity to differentiate yourself and reach new heights. Check out the Marketplace now at https://ow.ly/siRN50Rj7NP #MarketplaceListing #BusinessGrowth #ShowcaseYourExpertise #StandOut
Stand Out from Competitors and Showcase Your Expertise!
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From 2-4 December, join us at the ‘Medical Devices and Drug-Device Combination Products Workshop: Post-Market Surveillance and Clinical Evidence’ live-virtual training course. By joining this training course, you will be able to: 🔸 Enhance your knowledge on setting up a PMS system ang gain insights into the challenges and opportunities it presents. 🔸 Discover the critical link between PMS, risk analysis, and clinical evaluation to ensure the safety and performance of medical devices. 🔸 Learn from renowned representatives as they share their expertise and experiences. Don’t miss this great opportunity to stay ahead in the evolving landscape of medical devices and combination products. Register by 7 October to benefit from the early bird rate: https://bit.ly/3XTY7tq. Theresa Carlson Leon Doorn Josep Pané Miloš Stojković James Whitehead Sarina Zillikens Anna Amich #DIA #MedicalDevices #CombinationProducts #PMS #Learning