Leading the way in innovation are the biotech and pharmaceutical sectors, which use state-of-the-art technologies to improve patient care, medication creation, and medical research. These sectors have shown huge growth in the last ten years due to the demand for quicker, more effective clinical trials as well as regulatory compliance. Companies are looking for technical solutions that may improve stakeholder cooperation, guarantee data integrity, and streamline their operations due to the growing complexity of drug research and development.

Managing the enormous volumes of data produced during clinical trials is one of the main issues facing biotech and pharmaceutical businesses. To preserve adherence to legal requirements, guarantee patient data security, and improve trial results, the sector mostly depends on advanced software solutions. Businesses that invest in cutting-edge data management and automation technologies are well-positioned for success as digital transformation turns becomes a need rather than a luxury.

This is where Clinevo Technologies step in. Enterprises like these are reshaping the biotech and pharmaceutical landscapes by providing AI driven solutions, reducing operational inefficiencies and accelerating drug development cycle. Clinevo has certainly been a key player in optimizing clinical research and regulatory compliance.

Pioneering Digital Transformation in Clinical Research

Established in 2016, Clinevo is a software development company that specializes in creating and deploying reliable technological solutions for research and development in the life sciences. By employing cutting-edge technology like data warehousing, analytics, collaboration, automation, and artificial intelligence, they assist pharma, biotech, and CROs in cutting down on the duration and expense of clinical trials.

Clinevo is dedicated to providing the most effective and best-practice end-to-end software solutions with HIPAA, GXP, CSV, 21 CFR Part 11, and other relevant regulatory rules thanks to their special blend of domain knowledge and technological know-how. Delivering the greatest software solutions is made possible by their unparalleled domain experience and technological know-how.

By creating and deploying the most cutting-edge technologies, they hope to improve healthcare by cutting down on the time and expense of clinical trials. Their goal is to create a single platform for the clinical trials sector that facilitates data warehousing, analytics, collaboration, automation, and artificial intelligence throughout the clinical research enterprise.

Comprehensive Suite of Services

Clinevo offers a variety of detailed and cloud-based solutions designed to fit in with clinical trials. This helps a lot of pharma businesses to kick start their new drug trials and launch them before the deadline. Some of these services are:

Literature Management Software

An AI-enabled program called Clinevo Pharmacovigilance/Drug Safety Literature Management was created to help pharmaceutical firms, CROs, regulatory bodies, and healthcare institutions manage the enormous volume of scientific literature about drug safety and surveillance.

The features and functionality of Clinevo Pharmacovigilance/Drug Safety Literature Management software are specifically designed to meet the demands of pharmacovigilance including Automated Literature Search, Literature Screening and Prioritization, and Compliance Tracking.

Clinevo OneClinicalTrial Platform

Clinevo OneClinicalTrial is an integrated end-to-end Clinical Trials Platform that helps manage all aspects of clinical trials. It provides the following capabilities as an integrated platform to conduct Hybrid and Decentralized Clinical Trials:​

• Clinical Trial Management (CTMS)
• Electronic Trial Master File (eTMF)​
• Randomization and Trial Supply Mgmt. (IWRS)​
• Electronic Data Capture (EDC)​
• eCOA​
• eConsent​
• Remote Monitoring (rSDV)​

One Quality Management System (OneQMS)

Clinevo OneQMS is a cloud-based quality management system enables organizations to manage quality and compliance process digitally. OneQMS enables organizations to manage documents, training, Change, CAPA, audits in one place. It also complies with all current and emerging regulations including 21 CFR Part 11, ANNEX 11, GxP, and GDPR.

Clinevo Document Management System (DMS)

Clinevo Document Management System is a web based easy-to-use document management system to maintain, review, approve, manage, and publish your organization's documents electronically (including SOPs, work instructions, Contracts, Vendor documents, etc.) in one place.

Clinical Data Warehouse & Automation Console

Clinevo Data Warehouse is an easy-to-use, secured, regulatory compliance clinical trials data repository & warehouse to acquire, store, transform, consolidate, and report diverse data of clinical trials in one place. Moreover, the Existing clinical trials business team, technical team, and validation team can be trained in the Clinevo Clinical Data Warehouse / Clinical Data Repository within a week.

MICC Case Intake (PQCs, MIs and AEs)

Clinevo MICC Intake is a web-based tool for Medical Information Call Center (MICC) and PV users to Log, Track, and Monitor Product Quality Complaints (PQCs), Medical inquiries (MIs), and Adverse Events (AEs). Clinevo Pharmacovigilance Call Centre Intake sends automated email notifications to the consumers/reporters when there are updates from PV / Quality teams on the reported Product Quality Complaints (PQCs), Medical inquiries (MIs), and Adverse Events (AEs).

Mani Vasudevan | CEO

Mr. Mani Vasudevan brings over 20 years of expertise in Clinical Data Management and Pharmacovigilance. He led clinical trials, pharmacovigilance, and data management services while leading teams of managers, general managers, and vice presidents. His experience includes implementing GxP guidelines, BS 7799 (information security), ISO 9001:2008 (quality management), ISO 27001, 21 CFR Part 11 (electronic data security), HIPAA (protected health information security), Six Sigma (operational efficiency), and regulatory guidelines pertaining to Pharmacovigilance and Clinical Trial Services (CTS).

“We are committed to delivering the most efficient and practical end-to-end solutions. Our unmatched domain experience and technology expertise enable us to deliver the best solutions.”