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HomeServicesExtended Capabilities

ExtendedCapabilities

We offer more than core clinical trial services and we act as your strategic partner in navigating the Swiss life sciences ecosystem. Whether you are initiating a clinical trial, seeking to establish a presence in Switzerland, or aiming to expand your operations, we provide the connections and support necessary for success.

Our extended services include

Investigational Medicinal Product (IMP) Management

Coordinating the importation, storage, and distribution of IMPs in compliance with Swiss regulations.

Feasibility Assessments

Conducting local site and patient feasibility evaluations to validate study plans and optimize clinical development strategies.

Vendor Management

Identifying, qualifying, and overseeing third-party vendors to ensure quality and compliance throughout the trial.

Scientific Publications Support

Assisting in the preparation and submission of manuscripts and abstracts to disseminate trial results effectively.

Local Insurance Procurement

Facilitating the acquisition of mandatory local insurance coverage for clinical trials conducted in Switzerland.

Clinical Trial Registration

Registering studies on international and national platforms such as ClinicalTrials.gov and the Swiss Kofam portal.

Laboratory Services Coordination

Connecting clients with accredited local laboratories for sample analysis and other specialized testing needs.

Study Logistics

Coordinating clinical materials, shipments, and documentation to ensure seamless trial execution across all sites.

By leveraging our extensive network and deep understanding of the Swiss regulatory environment, GALSER ensures that your projects are well-supported from inception to completion. We are committed to facilitating your success in Switzerland's dynamic life sciences sector.

Faq

Business professional

Feedback from our clients

GALSER team has shown a great mix of professionalism, flexibility/adaptability and profound knowledge of the human research landscape in Switzerland
Big Pharma​
Medical Affairs Associate

01

/05

The GALSER team guided us through the Swiss regulatory process with clear advice and great responsiveness. Their support made the entire submission much easier than we anticipated.
Mid-Size Company​
Director Clinical Operations Europe

02

/05

A remarkable project leader who managed to deliver a high-quality protocol in a very short time
Swiss University Hospital
Principal Investigator - Initiated Investigator Trial

03

/05

Your level of detail and expertise really stand out. It’s been a real pleasure working together!
Start-Up​
CMO

04

/05

We were impressed by GALSER’s strong relationships with the study sites and their ability to keep things moving despite the usual challenges. It really helped us stay on track
Big Pharma​
Head of Global Clinical Development

05

/05

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