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- Regulatory life-cycle management of pharmaceutical products
- Submission of variations, PSURs, and new MAAs to Swissmedic
- Reimbursement of pharmaceutical products

- Installation of new pharmaceutical companies in Switzerland
- Provision of Qualified Person function for Good Distribution Practice (GDP)
- Writing of Standard Operating Procedures (SOPs)

- Compilation of bibliographic CTD dossiers
- Scientific writing
- Writing of GSASA reports
- Development of advertisement materials of pharmaceutical products
- Update and translation of SPCs / PILs / packaging materials

- Answering of medical queries by pharmacists and physicians
- Interim management, e.g. maternity cover
- Handling of pharmacovigilance in Switzerland
- Training of staff members, e.g. field force