Clinivance research & Innovations is a community of scientists and researchers committed to uncovering novel solutions to the world's most pressing problems in Health Care sector .
Clinivance Research & Innovations is specialized in site management for clinical trials. Our expertise lies in Clinical Research ,Medical Writing , Pharmacovigilance (PV) and clinical data management (CDM), ensuring that study sites adhere to protocols and collect high-quality data. We are dedicated to the detection, assessment, understanding, and prevention of adverse effects or any other medicine-related problems. Our comprehensive PV activities include prompt reporting of adverse events, monitoring and evaluating safety data, and implementing risk minimization measures. Additionally, our CDM team manages the collection, and analysis of clinical data to drive informed decision-making throughout the research process.
To provide comprehensive, innovative, and quality-driven clinical research solutions that ensure the safety and efficacy of pharmaceutical products. Our commitment is to uphold ethical standards while advancing global healthcare through efficient clinical data management, regulatory affairs, pharmacovigilance, clinical monitoring, and medical writing services.
To be a global leader in clinical research services, driving medical innovation and ensuring better health outcomes by delivering excellence in every aspect of clinical research. We strive to be the trusted partner for pharmaceutical companies, enhancing patient safety and promoting regulatory compliance.
"Efficient operational management to ensure the seamless conduct of clinical trials.
Thorough oversight to guarantee compliance with protocols and maintain the integrity of collected data."
"Accurate and compliant Documentation for regulatory submissions and clinical trial reports."
"Regulatory affairs services are tailored to ensure that clinical trials comply with all regulatory guidelines and align with international standards."
"Successful patient recruitment and retention are vital for the timely completion and overall success of clinical research."
Efficiently manage and analyze clinical trial data with precision and compliance.
Vigilant monitoring and reporting of drug safety throughout the product lifecycle
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