Expertise

Healthcare product development is a complex procedure to which you can’t not add simplicity, but we are here to help you take the complexity out.

We are keen to help the sector of healthcare grow and thrive using our expertise and experience. Our regulatory and health economic expert resources in the US and Europe have been supporting our clients with a wide range of services for the past 20 years.

All our expertises

Regulatory Strategy & Submissions

Design and implementation of global patient-centric regulatory strategies to ensure expedited product development leading to commercialization. Powered by a team…

Access to Market

Effectively positioning your product for the right indication from early stage of development. Have you considered the prevalence of your…

Clinical Research

Big enough to deliver and small enough to care HealthTech developers, including drug developers and medical device manufacturers are facing many…

Nonclinical and Clinical

Expect the unexpected Due to the increasing complexity of drug development and regulatory environment, the nonclinical and clinical plan, critical…

Chemistry, Manufacturing & Controls (CMC)

Overcome regulatory, scientific and technical challenges ensuring compliance, flexibility on the production capability and on-time delivery. A vital part of…

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Vigilance

From pre-market product safety to post-market surveillance, we provide integrated vigilance services all along your product life cycle. Safety of…

e-Publishing

VCLS assists life science companies to streamline the entire submission process from preparing eCTD compliant documents to electronic publishing and…

Due Diligence

VCLS assists investors and helps HealthTech product developers prepare for Due Diligences by providing targeted regulatory and value proposition assessments…