Welcome to SafeVig

Enabling Success through Comprehensive Clinical Research Solutions

At SafeVig, our end-to-end services will meet all your needs, through all phases of clinical trials. We are committed to improving patients’ health by collaborating with our clients. Our core team leverages extensive industry expertise and knowledge to provide clients with excellent services.

Every project is equally important to us. We first listen to your needs and strategize, aiming for a long-term partnership. We understand each project is unique where efficiency is utmost and accuracy is supreme for long-term success.

We have expertise in Clinical Trials involving drugs, vaccines, biosimilars, and medical devices. Our expertise comes from the experience of professionals having credentials to successfully conduct national and international clinical trials in every phase of clinical trial across different therapeutic areas.

Our Services

Clinical Operations

Clinical Monitoring

Medical Affairs

Regulatory Affairs


Clinical Data Management

Pharmacovigilance Services

Pharmacovigilance Technology

Our Solutions


The organization has transparency in its structure, workflow, and communication and a great team with global experience.

Highest Quality

We are committed to serving our customers’ requirements with a dedication to timelines and persistent flexibility standards.

Cost Effective

We provide cost-effective solutions that can be tailor-made to meet customers’ requirements.


We have robust scalability plans to meet the increasing demands of the industry.

We're your valuable partner.

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