Pharma IT’s Post

Acodis is excited to embrace the industry-led change highlighted in the recent DIA Global article about the power of reliance for post-approval changes. Our team recognizes the potential for AI to further enhance this process by bridging the gap between unstructured data and authoring tools, ultimately reducing the time-to-market cycle. We strongly believe in the power of AI to ease the burden of regulatory submission for CMC and clinical teams. Click the link below to learn more about how AI can benefit your regulatory submission process. #regulatorysubmission #CMC #Clinical #AI #timetomarket Link to the article: https://lnkd.in/esbGNUi8

How can #MedicalAffairs teams lead the charge in transforming data into actionable insights? From overcoming resource limitations to harnessing the power of #AI check out our blog recap of a recent Medical Affairs Professional Society (MAPS) webinar where industry experts shared best practices for managing complex data sources. ⬇️ https://hubs.la/Q02S4MNh0 #Pharma #MedicalExcellence #MAPSEvents

How can #MedicalAffairs teams lead the charge in transforming data into actionable insights? From overcoming resource limitations to harnessing the power of #AI check out our blog recap of a recent Medical Affairs Professional Society (MAPS) webinar where industry experts shared best practices for managing complex data sources. ⬇️ https://hubs.la/Q02S4MNh0 #Pharma #MedicalExcellence #MAPSEvents

A good discussion by Sameer Lal and Nikesh Shah on our Future Trends of PV report outcomes. Interesting to see that there is a noticeable trend - shifting from human-centric models to integrated man-machine solutions and pharma organizations are prioritizing proactive identification of events to enable faster decision-making.   Watch the complete video for detailed insights: https://lnkd.in/d5vQQ-XQ     #PVTrends #FutureReadyHealthcare #Compliance #Quality #Efficiency

#WebinarWednesday Please join RegDesk for our upcoming webinar with Regulatory Affairs Professionals Society (RAPS) on Wednesday, 25 Sep 2024 at 1:00 PM (ET) Advancing Medical Device Compliance Through Regulatory Management Systems and AI! Register Here: 👉 https://lnkd.in/gBBPZt3j Join our esteemed panel: Priya Paul (Bhutani) Bhutani: RegDesk, Founder and CEO Donald Ellis: Reva Medical, VP Quality and Regulatory Affairs Sue Dahlquist: Thermo Fisher Scientific, Senior Director Global Strategic Regulatory and Clinical Affairs Courtney Clark: Solventum, Senior Director Regulatory Affairs As they discuss: -How to manage increasing regulatory compliance burden -When regulatory teams should consider switching to a regulatory management platform -What teams should consider and what to expect when considering a change -How to create a business case for such an investment -Best practices to address change management -How AI can play a role in this #webinar #RAPS #RegDesk #RegulatoryCompliance #AI #changemanagement #bestpractices

Are you experiencing issues with data integrity, data quality, and data silos? Explore our recent project addressing these challenges for a biopharmaceutical company, including tackling siloed data, enhancing data transparency, addressing gaps in data comprehension, standardization, and implementing effective data governance strategies. Our approach emphasizes the need to adopt modern technology and foster data literacy. For a detailed discussion on the challenges, implementation process, and outcomes, please refer to the case study linked below. https://lnkd.in/dF6zaM9J Feel free to reach out to me (Nilesh Lahoti) any further discussion on our data product implementations at InfoCepts. #infocepts #ai #datanalytics #dataai #dataproduct #dataproducts

Navigate the vast world of medical literature effortlessly with DF Literature Monitor. Our AI-driven solution ensures precision, collaboration, and compliance for an efficient PV literature surveillance.   Experience the future of literature surveillance—empower your team with DF Literature Monitor. https://lnkd.in/gsnsszyH      #Pharmacovigilance #literaturesurveillance #literaturemonitoring #Safetyvigilance #DFLiteratureMonitor #ArticleDeduplication #NER #NERtechnology #E2B #datafoundry #healthcare #lifescience #LiteratureMonitoringsolution

Pharma confronts an influx of data and customer voices while new medications and biosimilars come onto the market every day. 5 challenges Pharma faces (and Authenticx helps solve) are: 👂 Listening to immense amounts of data 🏹 Limited accuracy in current listening metrics 🏁 Listening hurdles with regulatory guidance 🗯️Siloed integrations disrupt listening 📏 Lack of standardization in listening

Is your QMS ready with the #AI Act which was published in EU Official Journal? Make sure implementation dates are tracked to prevent any critical or major findings. #GMP #GLP #GCP #GDP #Valudation #Artificial Intelligence #AI #Pharmaceutical #Healthcare

Announcement to my colleagues in #LifeSciences who work in the #Quality #Compliance #GxP #CSV #IT and #Validation spaces. There is an upcoming webinar on July 10th at 11:00 AM EST brought to you by Fierce Pharma! 𝐓𝐨𝐩𝐢𝐜𝐬 𝐢𝐧𝐜𝐥𝐮𝐝𝐞𝐝: 𝘎𝘹𝘗 𝘶𝘴𝘦 𝘤𝘢𝘴𝘦𝘴 𝘸𝘩𝘦𝘳𝘦 𝘈𝘐 𝘪𝘴 𝘦𝘮𝘦𝘳𝘨𝘪𝘯𝘨 𝘘𝘶𝘢𝘭𝘪𝘵𝘺 𝘚𝘺𝘴𝘵𝘦𝘮 𝘱𝘳𝘢𝘤𝘵𝘪𝘤𝘦𝘴 𝘧𝘰𝘳 𝘮𝘢𝘯𝘢𝘨𝘪𝘯𝘨 𝘈𝘐 𝘪𝘯 𝘎𝘹𝘗 𝘛𝘩𝘦 𝘳𝘰𝘭𝘦 𝘰𝘧 𝘷𝘦𝘯𝘥𝘰𝘳𝘴, 𝘐𝘛 𝘢𝘯𝘥 𝘘𝘶𝘢𝘭𝘪𝘵𝘺 𝘪𝘯 𝘤𝘰𝘯𝘵𝘳𝘰𝘭𝘭𝘪𝘯𝘨 𝘎𝘹𝘗 𝘈𝘐 𝘐𝘯𝘷𝘦𝘴𝘵𝘮𝘦𝘯𝘵𝘴 𝘯𝘦𝘦𝘥𝘦𝘥 𝘵𝘰 𝘴𝘤𝘢𝘭𝘦 𝘈𝘐 𝘤𝘢𝘱𝘢𝘣𝘪𝘭𝘪𝘵𝘪𝘦𝘴 𝘪𝘯𝘵𝘰 𝘧𝘶𝘵𝘶𝘳𝘦 𝘎𝘹𝘗 𝘶𝘴𝘦 𝘤𝘢𝘴𝘦𝘴 Feel free to signup for FREE through the link below. One of the speakers for the webinar is our very own, President & Co-Founder, Bryan Ennis! https://lnkd.in/eGQM3Azz #FiercePharma #Webinar #AI #GXP #AIWebinar #GxPWebinar #PharmaWebinar #Pharma #Sware #Res_Q #Biotech #CDMO #CRO #MedDevice #QMS #Quality #QualityWebinar #QMS #LIMS #CAPA #GMP