A Whole Suite of Data-Driven Clinical Research Organization Services
Evolve Life is a notable and your ‘go-to’ CRO offering a whole host of clinical research organization services. Top-notch data is the real difference maker when it comes to clinical study & trials and at Evolve Life, we know how to strike the right balance for all stakeholders involved.
Strong scientific evidence based data is our forte and our whole array of services address your regulatory, scientific and logistical needs with sheer ease. Our CRO experts specialize in providing niche data driven clinical research organization solutions from inception to completion and even beyond.
Our CRO Services
Clinical Data Management
Optimize the value of your clinical data and transform the data management processes. Our clinical data management experts offer tailored concepts from concept report form, database locks, coding, SAE mana s not just in 2nd or 3rd phase trials, but late-phase approaches as well.
Our medical writing services include clinical study protocols, medical source review reports, clinical overviews & summaries, clinical study reports (inclusive of CSRs & SAE narratives), informed consents, investigator’s brochures, integrated clinical study reports compliant to ICH 3 and conference abstracts to name a few.
Ease various stages of drug development with our comprehensive and interdisciplinary strategy planning to acquire efficient regulatory pathways towards regulatory authorizations. Our whole gamut of regulatory compliance services covers all therapeutic areas.
We offer end-to-end clinical operations services starting from site feasibility to close-out. Our immensely experienced CRAs (Clinical Research Associates) render customized solutions including site selection, site monitoring and training, budget management for trials, source data verification and timeline management among others.
Count on our biostatisticians and SAS programmers for accurate statistical analysis. Get the much needed biostatistics support right from the start-up phase. Our services include clinical trials phase I to IV, Real World Evidence and Outcome Research. From study design to SAP, statistical consulting, statistical evaluation, randomization planning, regulatory support, and SAS programming apart from much more; we have you covered.
From planning, collecting raw data to securing it till data analysis is concluded, efficiently without compromising deadlines, quality and budget.The whole process is carried out under regulatory-compliant and disciplined methodologies. Our wellexperienced team of programmers and biostatisticians are here to provide expertguidance and consultation for statistical methodology, programming and generatingreports using the licensed statistical software to support interpretable outcomes.