Over the course of 2024, our collaboration with the ACCME enabled the transfer of over 770,000 CME credits to diplomate portals, bringing our total number of transferred credits to nearly 1.8 million since 2021. For information on how to participate in this process, see our website: https://ow.ly/Xtn850UMaJV
American Board of Surgery’s Post
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NABL (National Accreditation Board For Testing And Calibration Laboratories) NABL is an autonomous body under the Department of Science & Technology, Government of India, registered under the Societies Act. It was initially established to provide accreditation to testing and calibration laboratories, but later, its services were extended to clinical laboratories in India.
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👏👏Well done to everyone that took part in the recent #Alliance25 panel discussion: How to Navigate Accreditation Systems in Europe: EACCME and Beyond and especially our MD Yvonne Oliver 👏👏 As EBAC-Accredited Providers, PeerVoice are experts in developing European accredited CME. ✅ Yvonne Oliver, Caitriona Forde, Reinbert van der Fluit and Christopher Walsh are attending #Alliance25 and happy to answer any further questions you have about European CME. #EBAC #CME #EuropeanCME #MedEd
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Don't miss the latest issue of IFAPP - International Federation of Associations of Pharmaceutical Physicians & Pharm. Medicine with our Country Manager Dr Yasmin Nagaty writing an article about our recent conference " Pharmaceutical Medicine Domiciliation in the Middle East" held last month in Amman. Discover the key takeaways and insights from this important event. 𝐇𝐚𝐩𝐩𝐲 𝐫𝐞𝐚𝐝𝐢𝐧𝐠 📖 - https://lnkd.in/guS3eA8B #MEAPP2ndAnnualConference #IFAPPtoday
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We have officially received regulatory approval for our acquisition of HTLF. We look forward to further expanding our market presence to serve new and existing customers with more – more resources, more options, more support. Read the regulatory press release below for more details. https://lnkd.in/gNj6hZyX
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Let's come together and discuss on this important and transformation topic. looking forward.
Next week, join Sachin Dubey, Ph.D., at the A3P Switzerland Forum as he explores the critical role of establishing an Analytical Target Profile (ATP) in his session, “Establishing an ATP; An Essential Part of the Analytical Method Lifecycle.” Discover how implementing ATP throughout various project phases drives Quality by Design, ensuring precision and control in analytical development. Will we see you there? Event details: https://hubs.la/Q02QBcdK0 #A3P #KBIBiopharma
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i would like to share the link to 2 useful on line tools that may semplify the work of scientists working with recombinant monoclonal antibodies: 1) ABRSA ia simple and useful tool for antibody numberimg and cdr identification https://lnkd.in/d5jcgW6z 2) PLABDAB is a repository containing over 150,000 paired antibody sequences derived from patents and academic paper. it is vero usefull to underand if a mab sequence is patented or not. https://lnkd.in/daJfZ_K3 #mab #cdr #sequences #research #r&d
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For the first time as @EuroSIVA Chairman, conducting the Board Meeting! With great results: - 6th Porto Summer School in 20th-21st June 2025 - a draft of EuroSIVA statement against mixing drugs in the same sryringe - preparation of a consensus document on how to do TCI in 2024
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Exciting news! Our cybersecurity team is now equipped to support our clients with cybersecurity assessments aligned with MDR or FDA requirements. If you’re seeking assistance with cybersecurity compliance, contact us today! Did you know that cybersecurity is mandatory for medical devices under FDA regulations? At Eurofins E&E, we offer comprehensive services including gap analysis tailored to FDA cybersecurity requirements, preparing clients for premarket submissions, and guiding them through postmarket cybersecurity management. Reach out to us to ensure your medical devices comply with Section 524B of the FD&C Act and FDA cybersecurity guidelines. Let’s safeguard your innovations together! #Cybersecurity #FDACompliance #MedicalDevices
Our Notified Body team participates in the #NBCG-Med plenary meeting in Brussels: Aliisa Siljander, Laurence Matheron, Riikka Kylväjä and Paolo Dentis. 🇮🇹 Italy #MedicalDeviceRegulation (MDR) 2017/745 EUROFINS PRODUCT TESTING ITALY Srl / NB No. 0477* 🇫🇮 Finland Medical Device Regulation (#MDR) 2017/745 In-Vitro Diagnostic Regulation (#IVDR) 2017/746 Eurofins Electric & Electronics Finland Oy / NB No. 0537* *The current scope of accreditation for all EU Notified Bodies can be found on the EU #Nando website. The Notified Body Coordination Group - #NBCG-Med: ◾ Allows notified bodies to share experience and exchange views on the application of conformity assessment procedures and the activities of notified bodies. ◾ Promotes consistency among notified bodies and their processes ◾ Drafts technical recommendations and creates consensus on matters relating to conformity assessment and the activities of notified bodies ◾ Advises the Commission and the MDCG, at its request, on medical device legislation and its implementation ➡ More information about the European Commission: https://lnkd.in/dB9gA7S6 ➡ More information about Eurofins Electrical and Electronics (E&E) services: https://lnkd.in/eWW6YBZS 📧 Contact-Us: EE@eurofins.com
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Hello Medicos, Each and every Prometric exam is within reach if you just go through our MCQs. Crack your exam in first attempt. Here is the ultimate guide to prepare for Prometric exam. Please visit: https://lnkd.in/dKEt_uD3 #dubaiprometricexam #endocrinologistexam
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Hey Pharmily, I would like to learn more about the validity of NADAC. Does anyone know a SME who I can reach out to? How does NADAC factor in Chain vs. Independent pharmacy’s purchasing power? Thanks in advance.
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