Support is provided for the preparation of marketing authorization dossiers, management of variations, and technical documentation processes. Submissions are structured to ensure regulatory compliance and efficient progress.
Consultancy is provided for GMP inspection applications, manufacturing site authorizations, and batch release site application processes. All processes are managed comprehensively, from preparation to follow-up.
Support is provided for applications requesting prioritized evaluation of licensing and GMP processes. Applications are structured with strong scientific and technical justification.
Statistical support is provided for clinical and academic studies, including analysis, planning, and reporting. Comprehensive support is also offered for thesis studies and publication processes.
Readability studies are conducted to assess the clarity of Patient Information Leaflets (PIL). Where necessary, improvements and updates to the content are recommended.
Trust is at the core of Farma Team’s way of working.
Farma Team supports the effective and regulatory-compliant management of processes in the pharmaceutical and healthcare products sector, backed by extensive expertise and experience.
Farma Team provides reliable and consistent services through meticulous attention to detail, effective communication, and a robust internal quality system.
Farma Team adopts a comprehensive and holistic service approach, assessing processes from multiple perspectives and delivering practical, tailored solutions aligned with client needs.
Farma Team provides comprehensive consultancy and documentation support for the licensing processes of pharmaceuticals and other healthcare products.
Farma Team provides consultancy and documentation support for applications requesting prioritized evaluation and accelerated processing of marketing authorization submissions and GMP inspection processes by health authorities.
Farma Team provides consultancy and documentation support for inspection and application processes conducted within the scope of Good Manufacturing Practices (GMP).
Farma Team provides consultancy and implementation support for readability testing of Patient Information Leaflet (PIL) documents to assess their comprehensibility by end users.
Farma Team provides comprehensive consultancy and documentation support for pharmaceutical pricing and reimbursement processes.
Farma Team provides statistical consultancy and analysis services within the scope of clinical research and scientific studies.