Our service includes
Authorized Representative Services
Official representation of your company to conduct your clinical trial in Switzerland, fulfilling local legal and regulatory obligations.
Communication with Authorities
Liaison with Swissmedic, Ethics Committees, and relevant authorities, ensuring clarity, accuracy, and compliance in all regulatory interactions.
Regulatory Submissions and Documentation
Preparation, submission, and maintenance of all required regulatory documents, supporting approvals and ongoing compliance.
At GALSER, we offer reliable legal representation services ensuring excellent interactions with Swiss regulatory bodies.
Faq
Feedback from our clients
“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
01
/05
“Your level of detail and expertise really stand out. It’s been a real pleasure working together!”
Start-Up
CMO
02
/05
“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
03
/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
04
/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
05
/05
