The Silicon Review
In the competitive world we live in, clinical trials and other areas of pharmacology are gaining popularity. Clinical trials are essential as they determine the safety and effectiveness of new treatments, diagnostic methods, or drugs. Medicine or medical devices are closely monitored during clinical trials to ensure efficacy and safety. Clinical Management Softwares provide a suite of functionalities that makes it easy to manage a clinic.
Globally, there are many excellent software companies catering to the medical field, Clinevo Technologies stands out among them. Founded in 2016, Clinevotech is a Software Development Company specialized in developing and implementing robust technology solutions for Life Sciences R&D. It helps Pharma, Biotech and CROs in reducing their time and cost in Clinical trials by implementing innovative technologies that involves Data warehousing, Analytics, Collaboration, Automation, and Artificial Intelligence. With its unique combination of domain experience & technology expertise, Clinevo is committed towards delivering the most efficient and the best practical end-to-end software solutions with HIPAA, GXP, CSV, 21 CFR Part 11 and other applicable regulatory guidelines. Its unmatchable domain experience and technology expertise enables it to deliver the best software solutions. The vision is to Improve Healthcare by Reducing Time and Cost of Clinical Trials by developing and implementing the best innovative technologies. Develop a unified platform for Clinical Trials Industry that enables Data Warehousing, Analytics, Collaboration, Automation and AI across the clinical research enterprise.
Services offered by Clinevo Technologies
Clinevo Technologies provide IT consulting services to assist its clients with their ever–changing needs in the dynamic IT environment. The company’s goal is to help them to continuously improve the effectiveness & efficiency of their IT application environment by adopting and evolving towards re-usable software platforms. Cinevotech help clients analyze business and/or technology problems in order to identify and design platform based solutions. It also assists clients in planning their IT initiatives and transition plans. The biggest difference with Clinevotech is that it always strives for best results through close collaboration with its clients to understand their problems. The consulting team would become the extended IT team of the client and completely take over the ownership & responsibility of the end-to-end IT services.
With a combined experience of more than 15 years in the life sciences IT industry, Clinevotech will be able to suggest the software that is best suited for your needs. The company has extensive experience in evaluating, implementing and maintaining the best among the latest options available for your business. It helps you determine the exact requirements of your business. Clinevotech further assists you in choosing the product and vendor that shall meet your needs well within the framework of your budget. The right software creates a productive and cost-effective business environment so that all your focus can be on science. It assists you with the planning, analysis, configuration and validation of the solutions you purchase. By optimizing your implementation and validation process, Clinevotech ensures that you quickly begin your business with new software that meets your company standards and regulatory guidelines.
Clinevotech’s application developers plan and create customized, mission-critical applications that are unique to your business. The team invests quality time & efforts to assess your current business needs, in order to create an application that can be seamlessly integrated into your current workflow, greatly reducing the downtime associated with training. Much of the off-the-shelf software is built for the masses and sometimes it just isn’t sufficient. You need your custom, special application; because you have unique requirements and goals .Let the company’s application developers use their industry knowledge to deliver to you, the applications that match your requirements and specific business goals. Your business deserves an application that not only integrates itself seamlessly, but also makes your business operations more efficient.
Companies conduct data migration projects for many reasons: corporate events like mergers & acquisitions (many sources to many targets), new business models or processes (one-to-one), or to keep pace with technical progress or consolidating applications (many-to-one). Almost all migrations involve data transformations to get the data from one model to another. Transformation addresses data quality issues such as name-and-address cleansing, deduplication and standardization. Data is one of the most important assets that a company owns .It is collected and analyzed to create information for decision making. Data influences patient safety or product quality in Life Sciences. Clinevotech understands that if data is transferred to another data format or system, validation should include checks that ensure that the data is not altered in value and/or meaning during this migration process.
Data migration projects are often underestimated. Migrations are complex, as multiple data sources have to be harmonized and data quality is essential for Life Sciences compliant systems. To prevent costly future business process interruptions and to achieve compliance, it is recommended that all iterations should follow a clearly defined model. Clinevotech’s data migration experts deploy a number of approaches, products, as well as third party solutions to analyze the existing processes, plan the transition, obtain buy-in and migrate data, content & metadata to perform in-depth validations in order to ensure migration quality & regulatory compliance are intact.
Meet the Leader behind the success of Clinevo Technologies
Mani Vasudevan, Ph.D., Chief Executive Officer has over 20 years of experience in Clinical Data Management and Pharmacovigilance. Led a team of Managers / General Manager / Vice Presidents involved in Clinical Trials, Pharmacovigilance and Data Management Services. Expertise on Implementation of GxP Guidelines, 21 CFR Part 11 (Electronic data security), HIPAA (Protected Health Information security), Six Sigma (Operational), ISO 9001:2008 (Quality), ISO 27001, BS 7799 (Information Security), and guidelines pertaining to Clinical Trial Services (CTS) and Pharmacovigilance.