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Foto: Chloe Potter

Dr. Wolfgang Tüchler

I started my career in the pharmaceutical industry as a product manager more than 20 years ago. Since then, I have worked successfully in various international pharmaceutical companies and in different roles and areas of responsibility in Austria and Central and Eastern Europe  - from product manager to managing director of an Austrian branch.

 

Market access and patient access to innovative therapies have always been the focus of my activities - until today, when I make my experience and knowledge available to other pharmaceutical companies.

For me, market access management requires a holistic and multidisciplinary approach. My professional experience outside the pharmaceutical industry as managing director of a publicly financed start-up incubator in the state of Lower Austria or the leading medical publishing group in Austria helps me in my consulting work to bring in the necessary outside perspective of stakeholders, to enable access to decision-makers and to act as a mediator between the worlds, who understands and speaks the language of both public administration and industry.

I stand for competence and professionalism in order to achieve the best solutions for our customers.

Contact

+43 699 195 25 279

    • LinkedIn

    Dr. Franz Tüchler

    After studying technical chemistry, I have now been working as a consultant for the pharmaceutical industry in the GMP environment for more than 25 years in the following areas:

    • Sterile products (biopharmaceuticals, hormones, vaccines, plasma protein products, cytostatics)

    • Medicines, dietary supplements and cosmetics (solid forms, liquids, semi-solid forms)

    • Active ingredients

    • Veterinary medicines

    • Research institutions (drug development, vaccine development)

    • Medical devices - in vitro diagnostics

    • Hospitals (hospital pharmacies, clean rooms)

    Main topics:

    • Cleaning validation

    • Qualification of equipment, supply systems and clean rooms

    • Process validation

    • Method validation including method development

    • Environmental Monitoring

    • Quality management systems

    Activities:

    • Review of existing systems / GAP analyses

    • Building new systems / optimizing existing systems

    • Conducting risk analyses

    • Creation of documents (e.g. site master file, master plans, SOPs, plans, protocols, reports)

    • Planning, coordination and implementation of validations/qualifications

    • Support in the preparation of inspections and audits

    Contact

    +43 664 3463946

    • LinkedIn

    Contact

    We are always open to exciting and challenging projects. Contact us!

    +43 699 195 25 279

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