Quality Assurance, Regulatory Affairs
and Pharmacovigilance Services for Pharmaceutical Companies

Welcome to your pharmaceutical services partner for the Swiss market. We have been advising and supporting companies in Switzerland and abroad in all matters relating to quality, approvals pharmacovigilance of medicinal products, as well as other related product groups (food, cosmetic products and medical devices) since 1997.

 

Any questions?
Interested?

Contact us without any obligation:

 

T +41 44 787 70 20

Send email

 
Quality Assurance
A firm grip on quality at all times

Are you challenged with strengthening your quality assurance? Are you in the process of setting up or expanding your quality management system and would like technical support?

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Regulatory Affairs
Getting products authorised efficiently

Do you wish to have your product authorised for the Swiss market in the near future? Is adaptation of your EU dossier to Swiss requirements imminent?

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Pharmaconvigilance
Monitor adverse reactions

Are you planning to set up or optimise your pharmacovigilance system? Do you want to outsource the coordination of ADR reporting?

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Dr. Katharina Oehler

Scientific and Managing Director

Gabriela Betschart

Food, Quality and Regulatory Affairs Manager

Nunzia Carruba

Project and Administrative Associate

Danièle Chassot

Finance and HR Director

Christina Christen

Regulatory Affairs and Quality Specialist/Publisher

Arbër Destani

Regulatory Affairs and Quality Manager

Regula Felix

Lead Food, Cosmetics and Medical Device Services

Nils Fürrutter

Regulatory Affairs and Quality Specialist

Rahel Graf

Regulatory Affairs Manager

Elizabeth Heitzer

Lead Quality and Pharmacovigilance Services

Dr. Juana Kirsten

Senior Regulatory Affairs and Quality Manager

Ann Malone

Senior Regulatory Affairs Manager

Silvia Manser

Lead Regulatory Affairs Services

Dr. Kristin Wollenick

Senior Quality Manager

 
Experience and knowledge
have great value

We share our knowledge, in the form of tips and tricks from our experience, at specialist events, with checklists:

to the Know-How Box
to the events
to the checklists

About us
We have been committed to serving our clients - enthusiastically and cooperatively since 1997:

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Events

StartUp DRA 2025-CH - Modul 03: Zulassungsdossier – Chemisch pharmazeutische Dokumentation


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to all events
Hot Topics

Existing Obligations Despite Elimination of the RMP Requirement

RMP Requirement Eliminated – Which Obligations Remain for You?


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Services

Planning to enter the Swiss market?

Are you looking for support in developing a strategy to enter  the Swiss market? Or do you require advice on setting up a pharmaceutical company in Switzerland?


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