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HomeServicesStart-Up Activities

Start-UpActivities

Efficient trial start-up is critical for the timely and successful execution of your clinical study. We optimize the start-up phase through careful planning, effective coordination, and agile execution, ensuring your trial initiates rapidly and in full compliance.

We support you with

Study Feasibility and Site Selection

Careful identification, evaluation, and selection of qualified investigational sites tailored to your therapeutic and operational requirements.

Operational and Project Plans

Detailed and customized planning, clearly defining timelines, responsibilities, and deliverables to accelerate trial initiation.

Essential Document Preparation

Comprehensive preparation, collection, and management of all required regulatory and site-specific documentation, facilitating Swissmedic and Ethics Committee submissions and approvals.

Clinical Trial Agreements

Negotiation and finalization of site agreements, supporting swift onboarding of study sites.

Database Set-up and Validation

Implementation of robust clinical data management systems ensuring precise, timely, and compliant data collection from study start.

At GALSER, we proactively address potential hurdles early, ensuring your clinical trial starts effectively and remains on track from day one.

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

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

04

/05

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

05

/05

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