Our goal is to drive innovation and ensure the highest quality standards to bring your visions to life.

MedPharm Swiss AG is an independent, family-owned, full-service CRO (contract research organisation) providing the pharmaceutical industry, medical device manufacturers and academic institutions with a comprehensive range of CRO services.Headquartered in Lucerne/CH, our teams have successfully completed numerous projects with a wide range of indications. We are the experts in the planning, management and execution of national and international clinical trials and non-interventional studies. MedPharm Swiss AG has successfully managed monitoring in all European countries for many years in collaboration with partner CROs. We are the experts in all scientific, organisational and administrative aspects of clinical research. We only use state-of-the-art technologies and fulfil the latest standards.As a full-service CRO, we are able to respond quickly, efficiently and flexibly to individual requests, policies and processes.

MedPharm Swiss AG is the go-to for all tasks related to the organisation and planning of clinical trials. This includes active participation in the preparation of the Investigator Brochure as well as writing the observation plan or study protocol, handling submissions/notifications to the authorities (BfArM, Ethics Committee and National Association of Health Insurance Funds), database creation, randomisation, monitoring and data collection. Furthermore, the statistical analyses (biometrics or biostatistics) can be specified in a Statistical Analysis Plan (SAP). The medical statistics can be carried out after a plausibility check, and the study results can be summarised in a final report as part of the medical writing.

MedParm Swiss AG supports pharmaceutical manufacturers in setting up and monitoring pharmaceutical quality management systems (QMS) based on GDP and GMP guidelines.Of course, we also offer you quality systems for conducting clinical trials. Use our comprehensive SOPs, which fulfil all GCP/CTR requirements. We provide support with planning and documentation, with preparations for audits and inspections, help with adapting to changing framework conditions, check manufacturing processes (compliance check) and much more. MedPharm Swiss AG ensures that pharmaceutical companies have a quality management system that really suits them. Our consultants develop QM manuals and standard operating procedures (SOPs) in such a way that standardized processes reflect the individual workflows in the company. Appropriately and efficiently.

We support QM officers and specialized departments in the development of a highly qualified QM system and carry out a content review of existing systems and work instructions (SOPs). We prepare your team intensively for internal and external audits and offer support in the evaluation of your current quality management and the development of suggestions for improvement. Our certified lead auditors also carry out supplier audits or "independent" internal audits on your behalf.

Specifications, documentation, new research results and constantly changing regulatory requirements. MedPharm Swiss AG supports you in all stages of product development over many years: from the selection of active ingredients to the formulation of formulations and the development of the optimal composition and mode of action to the blinding of clinical trial samples and the production of development batches.

Products that have undergone a long and costly approval process need to establish themselves on the market as quickly as possible - also with the help of product design: Should your product be marketed as a medicinal product, medical device or dietary food? How should the product be structured? What shape and colour, size, flavour coating or even break edges can you use to make the most of the contact between patients or end customers when using your product? MedPharm Swiss AG offer you comprehensive advice on the marketability of your products.