PinnedFeatures to Look for While Choosing an eClinical PlatformAre you in a situation where you are planning to select an eClinical platform for your trials? You are not alone; many clinical research organizations are in the same boat. If you have ever scoured the internet to find out which Software to use for your clinical trials, you could…Eclinical Platform4 min read
Published in Clinion·Mar 24AIML and the Clinical Data ManagerThe Covid-19 pandemic has pushed the global clinical trial industry and regulators to rapidly adopt technology and accelerate clinical development. Along with other technologies, the adoption of AI & ML has moved forward at a much more rapid pace than initially envisioned. Similar to remote technologies, AIML technologies have gone…Ai In Clinical Trials4 min read
Jul 21, 2021Covid-19 Accelerating The Future Of Clinical Trials- DecentralizationFormulated on the advancements in the field of drug development, the pharmaceutical industry has been progressing at a rapid pace. But despite significant investments in the development of modern therapies and treatments, the overall efficiency of pharmaceutical R&D efforts have been declining steadily. …Clinical Trials3 min read
Jul 21, 20214 Benefits of Using ePRO During the COVID-19 PandemicThere are many benefits by using Clinion ePRO During the COVID-19 Pandemic During the ongoing COVID-19 crisis, CROs and Pharmaceutical companies are facing myriad of challenges. Many clinical trial studies have either slowed down or completely stopped due to the ongoing crisis. …Clinical Trials3 min read
Apr 12, 20213 Reasons Why Leading CROs & Pharma Companies are Choosing Us for COVID-19 Studies — ClinionWith COVID-19 unleashing catastrophe across the world, everyone is looking up to pharmaceutical companies to come up with a solution. Pharmaceutical companies are currently racing to create vaccines to slow down and potentially eradicate the ongoing pandemic. …Pharmaceutical4 min read
Apr 12, 2021Benefits of FDA 21 CFR Part 11 validationTo be compliant with US FDA 21 CFR Part 11 regulations, CFR Part 11 validation of electronic data management systems is mandatory. In simple terms, any computerized system involved in the clinical research process must comply with FDA 21 CFR Part 11. What is US FDA 21 CFR Part 11? …Pharmaceuticals Industry3 min read
Apr 12, 2021Benefits of a Clinical Trial Management System — ClinionClinion CTMS — Discover, Transform and Enhance your Clinical Trials Clinical Trials are a humongous undertaking. They involve massive amounts of data, hundreds of people and many sites for investigation. Managing these trials in the highly regulated clinical research field is challenging. …Ctms3 min read
Published in Clinion·Apr 8, 2021Implementing a Clinical Data Management System (CDMS) — ClinionClinion CDMS — Solutions to deliver high quality, quick and productive clinical studies We at Clinion understand how clinical data can completely impact the cost, effectiveness and turnaround time of any clinical study. Clinion’s Clinical Data Management System (CDMS) works towards storing and managing EDC and Paper-based data of clinical…Clinical Data Management3 min read
Published in Clinion·Apr 8, 2021Benefits of Electronic Data Capture — ClinionElectronic Data Capture(EDC) is used to help medical device and pharmaceutical organizations accomplish the greatest effectiveness with regards to entering data, structuring a database and conducting analysis for clinical trials. EDC technology has developed as past worries about data integrity through human error and connectivity issues caused by less reliable…Edc3 min read
Apr 8, 2021Benefits of Electronic Data Capture — ClinionElectronic Data Capture(EDC) is used to help medical device and pharmaceutical organizations accomplish the greatest effectiveness with regards to entering data, structuring a database and conducting analysis for clinical trials. EDC technology has developed as past worries about data integrity through human error and connectivity issues caused by less reliable…3 min read
