Velocious Clinical Research was founded with a vision to support the Pharmaceutical, Contract Research Organization, Medical Device, Nutraceutical, and Ayurveda industry to manage the asset “The Clinical Trial Data” through compliance process, expertise, competitive cost, uncompromised quality, and statistically sound data within the committed deadline that results into timely decision of Clinical Trial Outcome.
Our Clients rely on us for high quality, regulatory compliant data. our expertise is in designing, gathering, organizing, analysing, formatting and structuring the clinical trial data suitable for regulatory submission.
We have an experienced team who is expert in handling multi-centric trials across the globe.
Our procedures (SOPs) and Systems (Clinical Database) are in accordance with the current regulatory requirements and ready for audit. We truly believe our clients suggestions make our system more robust which sequentially helps us in providing the best services in-turn.
Clinical Data Management (CDM) is a critical phase in Clinical Research, which leads to generation of high-quality, reliable, and statistically sound dataRead More
With the increase in the data analysis and the changing regulatory era, this service is one of the most important aspects which provides an overviewRead More
Medical Writing is an integral part of Clinical Research and our Medical Writers work closely with stakeholders like Clinical Operation, Clinical DataRead More
Velocious Clinical Research under the roof of Standalone services provides a wide range of services in operating the clinical trials.Read More
We are proud to share the underlying values we take care of while execution of all our projects.
By qualification, he is a Bachelor of Homeopathy Medicine and Surgery (BHMS) and has done his Post-Graduation Diploma in Clinical Data Management (PGDCDM), with 14 + years of industry experience extensively in Clinical Data Management.
Throughout his career, he has worked with the most reputed Global Clinical Research Organizations and Pharmaceuticals companies wherein, he wasresponsible for revamping and establishing the Clinical Data Management processes in accordance with regulatory requirements & standards across the globe.
By experiences, he has worked on more than 112 studies from various therapeutic areas like Oncology, Patient PK, Psychiatric, Immunology, Vaccine, Gastroenterology, Metabolism, Dermatology, Metal Allergy, Ayurvedic, Nutraceuticals, Personal Health Care, etc.
His skills and interests are in Clinical Data Management and other Biometrics services, Subject Matter Expert (SME) for EDC software development, Medical Coding, CDISC-CDASH/STDM Implementation & review, follow Data Management standards and implement the new processes.