Services in drug approval, clinical trials and medical writing in Zurich and Bern
Stimolo Pharma Consulting provides comprehensive consultancy and support in pharmaceutical regulatory affairs, clinical studies and medical writing. With years of experience and a wide range of services, we guide your project from planning to implementation.
Your partner for drug approvals
From planning to coordination – we support you at every step of the approval process.
Our services:
- Planning, execution, and coordination of all necessary steps for national pharmaceutical regulatory applications
- Support with pharmaceutical licensing and renewal applications
With our expertise, we ensure that your regulatory applications are processed efficiently and in full compliance with regulations.
Expert support for clinical trials
We provide comprehensive consultancy and coordinating support for conducting studies in Switzerland.
Our services:
- Swiss sponsor representation for international studies
- Consulting and preparation of clinical trial applications for chemical active substances
- Planning, conducting and monitoring clinical trials
- Support with official procedures, e.g., with Swissmedic and ethics committees
Our goal is to ensure your clinical studies are conducted efficiently and successfully.
Scientific documentation at the highest level
Our team creates high-quality medical and scientific documents that meet the requirements of regulatory authorities and professional audiences.
Our services:
- Drug approval: CTD documents (e.g. expert reports) and regulatory submission documents
- Clinical trials: Study completion reports, study protocols and IMPDs
- Product Information: Preparation of Summary of Product Characteristics (SmPC) and Patient Information (PIL)
With precise and clear documentation, we support you in the successful communication of your research results.