Our Clinical Trial Management solution — designed to be a centralized Study Repository — has provisions for maintaining master entities and global objects that allow reusability across Clinical Trials. It forms the backbone of our Clinical Trial Platform, providing total control to System Administrators, Project Managers, and Clinical Data Managers to effectively maintain, manage, and monitor a study and operational database. We provide a set of tools that enables pharmaceutical organizations and CROs achieve speed and efficiency while implementing Software Solutions for their Clinical Trials.
Centralized System to Manage User Identities and Access
Our centralized User Administration service enables you to manage User Identities on our Platform and allows users to log in and access Study Resources. The unified sign-on feature simplifies access to our Platform’s various tools, facilitating Conditional Access to protect, govern, and engage with internal and external users more securely. Role-Based Authorization Control allows you to define roles centrally with granular levels of permissions that support the principles of least-privilege and segregation of duties.
Organization and Investigation Sites Master
We help you maintain a master for all Organizations you engage with and track their involvement in different Clinical Trials. Also, you can have a centralized database that lists Warehouses, Clinical Investigation Sites, Labs, Sponsors, CROs, Retention Facilities, Statistical Service Providers, and other Vendors to avoid repetitive processes in setting up Clinical Trials.
Unified Study Builder
Our Study Builder tools come with advanced features that allow you to define and configure the various processes and workflows needed for a Clinical Trial. Completely driven by Graphical User Interfaces — you can maintain the Study for even complex clinical trial designs including recent ones such as Adaptive Trials, Umbrella Trials, and Basket Studies. The Study Builder comes with versioning management to accommodate Study Amendments and Post-Production Changes in a centralized location within the tools, allowing targeted release across the Study, centrally or to individual Sites.
Global Clinical Data Libraries
Our Global Clinical Data Library provides a Centralized Form Library for CRFs, CDISC Libraries for Annotations and Controlled Terminology, and a central library for maintaining the Medical Coding dictionaries from MedDRA and WHO-DD. These libraries allow Clinical Data Management teams to build a comprehensive set of objects that can be reused across Clinical Trials, thereby reducing the setup time required for each Trial. All it takes is a few clicks for these objects to be imported into the Study Data design. Additionally, SyMetric is a Gold Member at the CDISC Community.
We have developed this function over the years based on our growing understanding of the monitoring needs of various stakeholders in Clinical Trials. As a result, this module provides the most comprehensive set of out-of-the-box reports that you can use directly to aid you in real-time monitoring of Studies and various other processes involved in a Clinical Trial.
Centralized Security and Compliance Manager
We firmly believe that Security and Compliance play a very important role in digital Clinical Trial Systems. Our centralized Security and Compliance Management tool on the Clinical Trial Platform allows Customers to define policies and drive security settings across various tools and modules based on their specific internal compliance and regulatory needs. Also, it comes with central auditability of data across the platform.
Founder and Managing Director
An entrepreneur with over 20 years experience in establishing and managing multiple business entities in various fields such as Life Sciences, Healthcare, and Social Enterprise, Uma started SyMetric in 2012. She plays a seminal role in all functions — from strategic decision-making to business operations. Under her leadership, SyMetric has expanded to US, Europe, and Latin America besides forging strong partnerships with Pharma Companies, CROs, and Technology Companies such as Microsoft, SAP, Tenthpin Management Consultants, and MINT Medical. She has been at the helm of Ladies Circle India (LCI) and is a member of several reputed organizations — Anthroposophical Medical Society of India, HIMSS India Chapter, 5HT Germany, NASSCOM, and SAP Industry Consortium for Life sciences.
A seasoned professional with over 34 years of experience in information technology and multiple industry domains, Raghuram is currently the Managing Director, India of Tenthpin Management Consultants. As part of Tenthpin’s global initiative, he is leading the efforts towards establishing a Life Sciences Innovation Centre in India. Enrolled in the Roster of Experts of WHO Digital Health Technical Advisory Group (DHTAG), he works very closely with the healthcare ecosystem in India. He has worked at SAP for nearly 17 years in multiple areas — Supply Chain-, Project-, Global Delivery-, Strategic Vendor-, Practice-, Product-, and Process Management. His guidance is integral to designing products, processes, and delivery models for enterprises in the Life Sciences and healthcare sector.
Ramesh Kumar T
Business Strategist and Mentor
A strategist known for digital dexterity and business acumen, Ramesh fits squarely into SyMetric’s vision. His entrepreneurial experience in the Software Industry extends to over 35 years. He has also made significant contribution to a large-scale Technology company. Business mentorship comes naturally to him, given his background as an entrepreneur, and he helps associates achieve success and growth.
Rahul Jayarama Reddy
A highly experienced software developer and project manager, his role in SyMetric is as diverse as his areas of expertise. He has 8+ years of experience in full-stack development of enterprise-level Cloud applications and has spent 6+ years in areas of Project Management and End-User Support. With sound knowledge of Data Management Practices, Designing, Business Process, and Process Validations in Clinical Trials.
Sai Siddharth is a leading policy strategist in the field of energy, environment, and climate change. He brings to the table innovative perspectives.
He is a Programme Associate at SED Fund, responsible for implementing and refining the grantmaking and program strategy and managing relationships with partners.
Sai previously was at J-PAL South Asia, where he led the Environment, Energy, and Climate Change sector. He was also interim lead for the financial inclusion sector and worked on the Cash Transfers for Child Health Initiative at J-PAL South Asia. He also worked at the National Health Authority in India, where he helped set up its Innovation Unit, and at the Government of Maharashtra (through a fellowship at the University of Chicago) on a water conservation program in the state.
Sai holds a Master’s degree in Public Administration from Columbia University and a Bachelor’s degree in Mechanical Engineering from RVCE in Bangalore.
Pranav brings SyMetric his deep expertise in the user interface. He ensures the technical feasibility of designs for superior product development and is responsible for UI across product suites. He is responsible for expanding and diversifying workflows across systems to enhance quality and efficiency.
Pranav is also an Audio Engineer with the experience of having engineered multiple covers and client compositions with a Recording time limit of 6 hours per song. Well-versed with client requests and their sheer energy ensuring their performance is not hindered.
Well-versed with – DAWs: Protools, Logic Pro X, Audio Cleaning software: RX 9, Avid S3, Analog boards, routing, and signal flow.
He is accomplished with tone matching, tonal balance, understanding compression + ADSR and Depth, process, and need for
mastering, and Ear Training.
He is continuously developing more efficient workflows with every recording and improving client interactions and interactions with his/her Environment.
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