PointCross Life Sciences @PointCross_LS
Solutions and Services for the BioPharma R&D Industries. pointcrosslifesciences.com Foster City CA, USA Joined July 2011-
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Struggling to meet SEND dataset submission standards? PointCross has you covered, we ensure: • 100% accuracy and consistency with GLP Study Reports. • Submission guarantee – no technical rejections. • A firm, fixed-price quote delivered in just 24 hours upon receipt.
Last week, we held a successful webinar: "The Most Common Issues in Preparing SEND." During this webinar, we dove into the most prevalent issues we’ve come across in SEND submissions and provided actionable insights on how to overcome them. Watch now: youtu.be/6reOpOZIhrA?si…
Join us on May 29th, 2024, at 12 PM EST / 9 AM PST for an upcoming webinar: The Most Common Issues in Preparing SEND. This webinar will be beneficial for industry peers that are involved in data submission and regulatory compliance. 🗓️ Register now: info.pointcrosslifesciences.com/webinar-issues…
Join our webinar on May 29th, 2024, at 12 PM EST / 9 AM PST! PointCross will cover The Most Common Issues in SEND. Save the date and register now: info.pointcrosslifesciences.com/webinar-issues… #SENDAssure #Webinar #PointCross #LifeSciences #Pharma #Biotech #CDISC #FDA #SEND
Visit PointCross at Booth #1537 to talk about your SEND needs. As one of the industry's leading and trusted SEND providers to over 275 Sponsors and CROs each year, PointCross offers 100% Submission-Ready SEND for your IND and submission needs. #2024SOT #ToxExpo #Toxicology #SEND
We are excited to meet everyone at the @SOToxicology conference in Salt Lake City next week! Drop by booth #1537 to meet our team members Rahul Madhavan, Cassandra O'Malley and Kunaal Madhavan #2024SOT #ToxExpo #Toxicology #nonclinical #preclinical #biotechnology
Wishing everyone a safe and happy holiday season! Biotech Hangout will return on January 5th. In the meantime, we invite you to register for our #Tweetup #Xup #JPM24 event on January 9th - all made possible thanks to our sponsors @JNJNews, @PureTechH, @FTIConsulting, @PointCross_LS, @BancofCal & @misprobiotech bit.ly/47Tr370
We’re excited to once again be hosting our #Tweetup #Xup #BiotechHangout event at #JPM24 thanks to our sponsors @JNJNews @PureTechH @FTIConsulting @PointCross_LS @BancofCal & @misprobiotech! Meet us at Persona (same location as last year) on Tuesday, January 9th from 7-10pm. RSVP now to be sure you’re on the list! bit.ly/47Tr370
We are thrilled to announce that PointCross Life Sciences has been recognized as one of the "10 Most Recommended Pharma & Life Sciences Technology Companies - 2023" by @cioinsiderindia Read more: hubs.ly/Q029CsXW0 #LifeSciences #Pharma #Innovation #CIOmagazine #Xbiom
Unlock the Power of Clinical Data Management (CDM) in Clinical Trials - Discover how CDM ensures data accuracy, quality, and compliance in our latest blog. Read more: pointcrosslifesciences.com/enhancing-clin… #ClinicalDataManagement #ClinicalTrials #MedicalResearch #DataIntegrity
PointCross is proud to sponsor the 2023 Orange County Biostatistics Symposium, where Sunil Gupta will chair the Data Science / Analytics component on Modern Analytics Tools and Processes and present on Better CDISC Standards with Metadata Programming.
eDataValidator (eDV) – Your Ultimate Data Validation Solution. Ensuring accuracy in Clinical SDTM, ADaM datasets, and Nonclinical SEND data is now easier than ever. Discover how eDV transforms data validation! Read more: pointcrosslifesciences.com/validation-for… #SDTM #ADaM #SEND #eDataValidator
Generating high-quality SEND data can be challenging, as it requires careful mapping of data to the appropriate SEND domains and ensuring data quality and consistency. Read full article: pointcrosslifesciences.com/send-data-stan… #FDA #SEND #Nonclinical #CDISC #CBER #CDER #CRO #Toxicology #Sponsor
🔬 Explore the significance of clinical trials in drug development and patient care. Our latest blog post delves into their purpose, types, and phases, shedding light on their role in shaping medical advancements. pointcrosslifesciences.com/understanding-… #ClinicalTrials #DrugDevelopment
Watch our recent webinar on eDataValidator - a comprehensive tool for validating SDTM trial data against regulatory rules. Learn to efficiently validate datasets, generate SDRG, and more. Link: pointcrosslifesciences.com/edatavalidator… #DataValidation #ClinicalTrials #fDa
Join us for a 30-minute walkthrough of the eDataValidator (eDV) tool. Register for the webinar using the links below: EU: info.pointcrosslifesciences.com/edv-webinar-eu US: info.pointcrosslifesciences.com/edv-webinar-us #FDA #CDISC #SDTM #ADaM #clinicalresearch #biotechnology #lifesciences #PMDA #clinical #nonclinical
Join us for the 30-min walkthrough on eDV that allows users to validate an unlimited number of datasets either on a secured cloud environment or on a locally hosted, offline desktop tool. Link: EU: info.pointcrosslifesciences.com/edv-webinar-eu US: info.pointcrosslifesciences.com/edv-webinar-us
#PMDA released validation rule v4.0 for SDTM/Define.XML in Feb 2023. #PointCross implemented it on 28th Apr 2023. PMDA Validator Rules v4.0 supports #SDTM IG v3.3 & removes Define.xml 1.01 support.
PointCross is thrilled to be hosting #PHUSE SDE on August 10th, 2023. This PHUSE SDE theme will review the scope, technology, and process to better understand and define best practices in clinical data ingestion, harmonization, and analysis. Learn more: bit.ly/3KXy64q
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