Our services include the areas of the responsible person, quality management, development, regulatory affairs and pharmacovigilance.
Our experience covers all GDP and most GMP-relevant tasks of quality management, such as audits of suppliers and service providers or editorial work (Site Master File, Periodic Safety Update Reports, Stability Reports, Product Quality Reviews ….).
Development and regulatory affairs are our core competence. In the past decades Phytocon has help go get the approval of about 30 marketing authorizations in Switzerland. In addition to editing the expert reports on quality, safety and efficacy, we have organized pharmacological research and about 10 clinical trials. Some of these studies have been published.
We are particularly interested in bibliographic research with a focus on phytotherapy. In November 2017, e.g. an article on clinical findings on cannabidiol appeared (DOI: 10.1159 / 000484886).