We are the experts in gathering, organizing, analyzing, formatting
and structuring of clinical data for regulatory submission.

We support our clients in seamlessly analyzing the clinical data by integrating expertise and technology resulting in a right time decision of Clinical Trial Outcome. Clients rely on us for high quality, regulatory compliant data. We are the experts in gathering, organizing, analyzing, formatting and structuring of clinical data for regulatory submission. We have an experienced team of Clinical Data Management handling multi-centric trials across the globe.

At ClinVigilant, we provide cost-effective solutions without compromising the quality and committed timelines to ensure that our clients have accurate data information to take critical decisions on time.

Our procedures (SOPs) and Systems (Clinical Database) are in accordance with the current regulatory requirements and are ready to invite our clients to audit our systems. We truly believe our clients suggestions make our system more robust which sequentially helps us in providing the best services in return.

project Management

Clinvigilant Research provides skilled project managers that are well suited to the needs of clinical trials. With an average tenure of 10+ years in the industry..

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Data Management

Our databases fulfill important baseline attributes while allowing for the specialized configuration required for regulatory report outputs, and are configured with..

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Biostatistics

Our biostatistical staff members provide more than data analysis; they have in-depth knowledge of the methods for studying and the techniques that are used to analyze..

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monitoring

Clinvigilant Research monitors have experience with both outpatient and inpatient records and procedure notes. Monitors are also trained in control response reduction..

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questions

ClinVigilant provides inclusive regulatory operation services to Pharmaceuticals (FP and API), Biopharmaceutical, and Healthcare, CMO and Clinical Research industry..

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writing

Clinvigilant Research medical writers are experienced in both clinical and regulatory writing techniques to provide concisely written documents that exceed client expectations..

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quality

As a part of quality assurance activities, we improve the reliability of clinical studies, post-marketing clinical studies, clinical research etc. by evaluating and verifying compliance..

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validation

Many regulated companies, such as those in life sciences, food and beverage, and the cosmetics industry, worry about time and resources required for software validation..

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CRO Setup

We can help you to setup/establish new BE centre /CRO/ bioanalytical lab/clinical facility. We have decades of experience in BE centre setup. We can give end to end BE centre setup support..

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