Streamline your clinical operations and make clinical research easier
We are a true cloud venture that provides collaboration in clinical research between sponsors, CROs, and clinical sites by varied range of clinical solutions.
Accelerate clinical data capture with the right insights
Our connected suite accelerates data capture with a real-time centralized solution, monitors compliance and meets regulations on time and within budget.
Overcome challenges, Uncover
new paths
Get your clinical trial back on track with our time-trusted tools and services.
Explore Our Offerings
that puts you on the fastest path to success
We innovate and deliver amazing product line we constantly strive to enhance
our offerings that satisfy clients’ needs.
Computer System Validation of Compliances
Healthcare and Clinical trial application validation for compliances like PII, PHI, HIPAA, SOC2, 21CFR, Data Privacy 11 etc. End-to-End Regulatory & Compliance Management
Design, Installation, Operational and Performance Qualification (DQ, IQ, OQ, PQ)
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Cloud Migration, Application Monitoring & Management
Cloud Migration and Compliance
24x7 Clinical Trial and Healthcare Application Monitoring, Maintenance
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System Integration, Data Migration, Extraction & Curation
Systems Integration with Applications in Healthcare and Clinical Trial Ecosystem and third-party applications Including Financial Applications and Inventory Tracking system
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System Setup for study startup and Pharmacovigilance
Study Setup for EDC (including Design Studies for EDC, CRF Creation, Edit Checks and Assessment Schedule) & Pharmacovigilance System and Safety Signal Management Systems setup
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Professional and Consulting Services
Team of SMEs, Solution Architects, Business Analysts, Frontend and Backend Developers (React JS, Python, Full Stack) and QA for quick Clinical Trial Applications ramp up.
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Application Implementation, Migration & Upgrade Services
Development, Implementation & Maintenance of Clinical Operation Management Applications (Veeva Vault, IQVIA Trial Management and Data Analytics Suites, & Oracle & custom applications)
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Analytics, AI/ML, eCOA, Trial Supply Tracking and Management
Clinical trial Feasibility Study, Outcomes prediction, real-time material tracking etc.
Schedule a Discussion with the ExpertsOne Of The Innovative And Leading Clinical Research Services And Technology Solution Providers
Offering our Customers a Full Spectrum of Professional
and Managed Services
Our commitment is to ensure that clinical trials are both safe and expedient, simplify your regulatory affairs, and assist you with managing quality and learning activities.
Clinical Operations
CTMS
eTMF
EDC
eCOA
RTSM
Regulatory Information Management
Registrations
Submissions
Submissions Publishing
Submissions Archival
Quality Management
System
QMS
Quality Docs
Learning/Training
Management System
Curriculum management
Quality event management
Quality lab operations – SOPs, CC forms
Unique Perceived Benefits With Us
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Supports you with prospective, ongoing and retrospective management of clinical trials
Provides unified access to various stakeholders participating in clinical trials
Streamlines clinical trial operations with a smart and efficient document management system
Manages master data for contacts, sites etc., using our master data management system
Monitors and gains complete visibility and control over all clinical processes
Significant reduction in the study set-up time, increased accuracy of auto-classification, and reduced reconciliation time.
Why Smart IMS
24/7 Monitoring and maintenance of your clinical applications with real-time notification on process and services disruption or failure.
Cost effective Opex & SaaS model and customized Capex model for application services fitting in your requirement and budget.
Experience and expertise to streamline the process and capitalize on cross-departmental efficiencies.
From site identification to Study close-out, we oversee and manage complete clinical operation.
Fully Compliant Solutions with 21CFR Part 11, Annex 11 and HIPAA regulations
Improved site/study management aligned to amendments, protocol, and subject deviations.
Diverse team of clinicians, medical, technology experts and process engineers to help run your trials and manage the processes, site and patient data.
Dr. Rahul Srivastava is responsible for Strategy, execution, and P&L for the Life Sciences portfolio at Smart IMS, focusing on technology solutions and services for CROs, AROs, Pharma, life sciences, and regulators.
Dr. Srivastava is coming with over 25 years of experience in technology implementation in life sciences and dental sciences. As a thought leader, he carries a business-oriented consulting experience to help the client in the process re-engineering and building cost-sensitive and robust technology solutions.
Dr. Srivastava has been a part of various IT governance and steering committees involving CIOs and CTOs of client organizations to advise on product strategy, and IT TCO analysis for capital budgeting, planning, governance, and partnership selection.
Dr. Srivastava is a published author, trainer, and a coach.
Dr. Ritesh has over 19 years of experience working with CRO, Healthcare IT, BPO and Government Organizations. He is leading the development of the Life Sciences Product portfolio and solutions.
Dr. Ritesh comes with a blend of technology and Domain expertise and has worked on various functions including Service Delivery Operations and Subject Matter expertise for Pharmacovigilance, Clinical Data Management and Healthcare Product development. Ritesh also comes with experience of implementation of Electronic Health Record Application and providing leadership for implementation of Government schemes at State level.
Dr. Alex Philip is a Technologist and Product Strategist with extensive expertise in Lifesciences - Clinical Trials, and Healthcare, in both the Providers and Payers space.
He is a trained Physician with prior clinical experience and has nearly two decades of experience in developing solutions for Clinical Operations, Clinical Data Management, Electronic Trial Master Files, Electronic Health Records, and Payer Systems. As a subject matter expert, he has executed several successful product strategies to develop solutions that meet customer needs and drive business growth.
Dr. Philip is passionate about leveraging technology to improve patient outcomes and has specific expertise in Healthcare Interoperability and Systems Integration. With his strong background in Product Development, Product Design, Technical Architecture, and Business Analysis, he is well-versed in identifying and implementing emerging technology trends and their potential impact on the market.
Dr. Philip's unique blend of medical expertise and technology allows him to innovate and improve healthcare delivery.
Former FDA Oncology Division Director
Drug approvals in > 10 novel indications
1st approval of PARPi, CDK4/6i, and immunotherapy in breast, gyn, gu cancers
Architect of Oncology Center of Excellence
Principal Investigator of multiple research programs
Former AstraZeneca Executive Leadership Committee
Global Head of Oncology Regulatory
Global Medicines Lead, Women’s Cancers and Novel combinations
Founder, Applied Innovations at BeiGene
Co-Inventor of FICS Technology
Ex Associate Investigator, National Cancer Institute
Founder, Hematology Oncology Safety Net Providers
Harvard- and Columbia- trained physician scientist
Former Harvard Faculty, Physician, and Researcher
Attending Dermatologist, Massachusetts General Hospital and MGH Melanoma and Pigmented Lesions Center
Investigator, Wellman Center for Photomedicine
Former Head of Oncology Regulatory Science and Innovation at AstraZeneca
Howard Hughes Medical Institute-National Institute of Health Research Scholar
Co-inventor of FICS technology
Consultant/Advisory Boards: MediVis, Buoy Health, Worldcare Clinical, AlleyCorp
