Our Services

Clinical Development

Regulatory Submission

Our regulatory team is comprised of regulatory specialists with experience of working with regulatory authorities in Europe, USA, Middle East Asia and Japan

Project Management

Our Project Management Model ensures sponsors' needs are met by utilizing best-in-class project management solutions.

Medical Writing

We prepare quality medical writing deliverables for you with the right key messages for regulatory documents.

Medical Monitoring

We have a team of experienced clinicians who have vast experience of managing clinical trials.

Feasibility and Site Selection

Identifying, screening and qualifying investigational sites is an ongoing challenge for every clinical trial team.

Data Management

Our data management staff includes clinical data managers, database developers, data entry specialists, medical coders, biostatisticians and we have extensive systems’ support capabilities.

Clinical Trial Monitoring

We offer deliverable based clinical monitoring services to manage clinical trials on time and within budget. Our experienced monitors manage clinical trial by implementing technology based solutions to provide efficient services…

Biostatistics

Our biostatisticians have the expertise to support your needs in clinical development, including statistical planning and data review.

Post-Authorization

Risk Management

Recognizing the fact that benefit-risk balance is periodically reviewed by the regulatory authorities and that many.

Post Approval Studies

At VST Research, our understanding of the complex post-approval environment combined with decades of experience…

Pharmacovigilance

VST helps clients proactively meet regulatory requirements throughout their product's life cycle.

VST Research Consulting

Functional Service Provider

We have a diverse team of experts, ranging from local clinical research associates as well as key opinion leaders,

Training

Our consulting practitioners span the entire product development and delivery continuum.

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