MAC Clinical Research’s Post

Investigational sites are the crux of clinical trials, providing essential data, patient recruitment, and procedure execution. Discover how the critical CRA/CRC relationship drives trial success through respect, professionalism, transparency, and collaboration in the April 2024 issue of Clinical Researcher. Read more > https://bit.ly/3UV5VaX #ClinicalResearcher #ClinicalTrials #ClinicalResearch #SiteRelationships #Sponsor #CRO

Looking to partner with a CRO for your clinical trial? It's important to understand the differences between specialist and full-service CROs. While full-service CROs offer end-to-end support, specialist CROs can offer greater agility, personal attention, and access to senior expertise. Don't settle for a 'one-stop-shop' - read our latest blog to find out what to look for in a CRO. Link in comments to read. #ClinicalTrials #CRO

https://clinfinite.com/ 🔷 Clinfinite Solutions is your trusted Research & Development partner, specializing in ICH-GCP compliant Clinical Research Organization (CRO) services. 🔷With a commitment to excellence, we offer end-to-end solutions for clinical trials, ensuring adherence to international quality standards. 🔷Our dedicated team of experts brings extensive experience in designing, managing, and executing clinical trials across diverse therapeutic areas. 🔷We prioritize precision and efficiency, providing comprehensive support to streamline your research process. 🔷From protocol development to regulatory submission and site management, Clinfinite Solutions is equipped to navigate the complexities of clinical trials. 🔷We emphasize data integrity and patient safety, employing cutting-edge technology and robust quality assurance practices. 🔷Our client-centric approach ensures transparent communication and tailored solutions to meet your unique research objectives. 🔷Choose Clinfinite Solutions as your CRO partner, and let us collaboratively advance your research endeavors, bringing innovation to healthcare with ICH-GCP compliance at the core. #ClinfiniteSolutions #ClinicalResearch #CRO #ICHGCPCompliance #ClinicalTrials #ResearchAndDevelopment #HealthcareInnovation #PatientSafety #DataIntegrity #RegulatoryCompliance #ClinicalTrialManagement #ProtocolDevelopment #ResearchPartnership #QualityAssurance #GlobalHealth #ResearchExcellence #InnovativeHealthcare #CollaborativeResearch #ClinicalOperations

Sponsors, #clinicalresearch Sites and #CRO's - We can support you in ensuring that all your clinical research professionals working on your studies are independently competence verified and #qualityassured in ICH #gcp, against the global best-practice standards set by the Industry. If you would like to speak to us about accrediting your #workforce and demonstrating 'confidence in competence' of your staff to the industry, please do get in touch. You can find out more about our industry leading ICH-GCP Accreditation here: https://lnkd.in/ehyqezTe #clinicaltrials #qualitymanagement #clinicalstudies

#GCTC We are Excited to welcome our Gold Sponsor NWEH for our Global Clinical Trials Connect 2024 this May in London, UK. #GCTConnect NWEH's platform ensures a clinical trial that is true-to-life, giving sponsors real results by testing innovative healthcare therapies with those who need them most, anytime, anywhere, ensuring patient safety at every stage. To learn more about NWEH, visit their website at https://www.nweh.co.uk Conference Website: https://lnkd.in/gpPRS9Bw Registration link: https://lnkd.in/gU6fsHUH For Queries and Team Discounts please email at info@corvusglobalevents.com Email us at sponsor@corvusglobalevents.com for more information on Sponsoring/Exhibiting/Speaking opportunities. #primarycaretrials #patientrecruitment #hybridclinicaltrials #smartclinicaltrials #improvinglives #patientcentricity #Patientcentricity #SiteSelection #decentralizedtrials #ClinicalDevelopment #vendormanagement #riskbasedmonitoring #clinicalauditing #FutureTrials #Clinicalinnovation #Clinicaloperations #ClinicalDesign #patientengagement #ClinicalTrialAuditing #vendormanagement #Clinicaltrialsbudget #Clinicaltrialsoutsourcing #ClinicalDataManagement #CRO #ClinicalTechnology #ClinicalTrialAgreement #realworldevidence #patientdata 

✨ FDA’s Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors August 2023 ✨ … This guidance is intended to assist institutional review boards (IRBs), clinical investigators, and sponsors in complying with FDA’s informed consent regulations for clinical investigations. This guidance supersedes FDA’s guidance entitled “A Guide to Informed Consent,” issued in September 1998, and finalizes FDA’s draft guidance entitled “Informed Consent Information Sheet,” issued in July 2014. This document is structured to first present general guidance on FDA’s regulatory requirements for informed consent and a discussion of the roles of IRBs, clinical investigators, sponsors, and FDA related to informed consent, followed by a series of frequently asked questions. IQVIA Ammad Fahim Bushra Anwar Sumeyya Ahmed (Formerly Sumeyya Azam) Dr Saboora Waris Prof. Dr. Ume Sughra Sajjad Ali IQVIA Research & Development Solutions #irb #clinicalresearch #clinicaltrials #cro #clinicalresearchassociate #clinicaltrialmanagement #informedconsent

Overcoming Obstacles to Clinical Trial Recruitment and Retention https://buff.ly/3FVY5Hc #clinicaltrials #clinicaltrialrecruitment #clinicaltrialretention #clinicaltrialsites #trialsites

🔬The UK is moving forward with the long-awaited revision of its clinical trial framework!   The MHRA launched a notification scheme for low-risk clinical trials:   ◻ 50% reduction in the review time for the lowest-risk phase 3 & 4 trial applications (14 days instead of 30) ◻ First in human, phases 1 & 2 and amendments are currently excluded from the scheme scope ◻ 20% of all clinical trial applications could be eligible for the new review pathway https://bit.ly/3FauqK5   #UK #Clinicaltrials #Medicines

Over two decades, PharmaSols has cultivated expertise, built strong relationships, and developed innovative strategies that have positioned us as the premier CRO in Australia and New Zealand. What’s the secret behind our growth? It’s not just about navigating the clinical trial landscape; it’s about a relentless commitment to excellence, our adaptability to evolve with the industry, and our unwavering focus on delivering high-quality clinical data for global sponsors. Watch this video to see how we've grown to be the trusted partner for sponsors looking to run successful, efficient, and compliant clinical trials down under. #PharmaSolsJourney #LeadingCRO #ClinicalTrials #ANZHealthcare #IndustryLeadership #ClinicalResearch

There is much confusion with sponsors and CRO's on IOR requirements and options. As many vendors are starting to offer this service, limitations and legal verbiage must be ironed out. It's not a simple quick process. I continually have conversations with companies that need this service but are caught off guard by why it's such a big deal. Clinigen offers THis service and many others to assist with your Clinical Trials. https://lnkd.in/eBvxfmHd