Our service includes
Inspection Readiness Assessments
Detailed evaluations of trial sites and processes, proactively identifying and addressing compliance gaps to ensure inspection readiness.
Preparation and Training
Targeted training and support to site teams and project staff, ensuring clear understanding of expectations and effective responses during audits and inspections.
Corrective and Preventive Actions (CAPAs)
Development and implementation of targeted corrective action plans, ensuring effective resolution and ongoing compliance post-audit.
At GALSER, our proactive and structured approach to inspection and audit readiness gives you assurance and peace of mind, reinforcing compliance and quality throughout your clinical research.
Faq
Feedback from our clients
“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
01
/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
02
/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
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
