Marti Farm
Marti Farm is a Croatian company supporting pharmaceutical, biotechnology, medical devices, food supplements, cosmetics, and healthcare industries. They provide core services including pharmacovigilance, registration, market access, clinical trials, patient support programs, and medical writing. With over 10 years of experience, they are recognized as a reliable partner and are ranked among the top 10 pharmacovigilance consulting companies in Europe. They focus on continuous development and expertise to add value for their clients. The company also specializes in services related to antimicrobial resistance, aromatherapy, eCTD dossier submission, and clinical trials, emphasizing regulatory compliance, safety monitoring, and innovative solutions.
Industries
Nr. of Employees
small (1-50)
Marti Farm
Products
Cloud-accessible pharmacovigilance case management software
Cloud-hosted pharmacovigilance database and case-management system supporting intake and processing of adverse event cases in multiple regulatory formats, integrated literature monitoring, activity reporting and web/mobile access.
Ispitivanje razumljivosti upute o lijeku
Usluga ispitivanja razumljivosti upute o lijeku za farmaceutske proizvode.
Sympto
A pharmacovigilance safety application upgraded in accordance with the latest industrial regulations and ISO IDMP standards of the EU.
Farmakovigilancija
Usluge kliničkog praćenja sigurnosti lijekova, uključujući prijavu sigurnosnih informacija regulatornim tijelima i pripremu Izvješća o neškodljivosti lijeka u razvoju (DSUR).
Farmakovigilancijske usluge
Usluge praćenja sigurnosti lijekova koje pokrivaju prikupljanje, pregled i procjenu podataka uz validirane postupke i ISO 9001:2015 standard.
Usluge pružanja medicinskih informacija
24/7 usluga pružanja medicinskih i znanstvenih informacija prilagođena specifičnim zahtjevima klijenata, namijenjena odgovaranju na upite zdravstvenih radnika, pacijenata i šire javnosti o lijekovima, medicinskim proizvodima, dodacima prehrani i kozmetičkim proizvodima.
Cloud-accessible pharmacovigilance case management software
Cloud-hosted pharmacovigilance database and case-management system supporting intake and processing of adverse event cases in multiple regulatory formats, integrated literature monitoring, activity reporting and web/mobile access.
Ispitivanje razumljivosti upute o lijeku
Usluga ispitivanja razumljivosti upute o lijeku za farmaceutske proizvode.
Sympto
A pharmacovigilance safety application upgraded in accordance with the latest industrial regulations and ISO IDMP standards of the EU.
Farmakovigilancija
Usluge kliničkog praćenja sigurnosti lijekova, uključujući prijavu sigurnosnih informacija regulatornim tijelima i pripremu Izvješća o neškodljivosti lijeka u razvoju (DSUR).
Farmakovigilancijske usluge
Usluge praćenja sigurnosti lijekova koje pokrivaju prikupljanje, pregled i procjenu podataka uz validirane postupke i ISO 9001:2015 standard.
Usluge pružanja medicinskih informacija
24/7 usluga pružanja medicinskih i znanstvenih informacija prilagođena specifičnim zahtjevima klijenata, namijenjena odgovaranju na upite zdravstvenih radnika, pacijenata i šire javnosti o lijekovima, medicinskim proizvodima, dodacima prehrani i kozmetičkim proizvodima.
Services
Consultancy to implement quality management systems, lead-auditor services and accreditation/certification preparation including medical device readiness, pre-inspection audits and CAPA development.
Outsourced pharmacovigilance operations including case intake and processing, regulatory reporting, literature monitoring, PV system audits, inspection support and signal management for marketed products and clinical trials.
Preparation and submission of regulatory dossiers, liaison with competent authorities, MAH support, renewals, variations, labelling and packaging text services across medicinal products, medical devices, food supplements and cosmetics.
Full-service clinical trial support including project management, monitoring, site feasibility and qualification, logistics for investigational products and supplies, patient recruitment support and preparation for regulatory inspections.
Design and management of patient support programmes, including nurse-led education, adherence monitoring and multi-channel patient engagement.
Creation and review of regulatory and promotional documentation, preparation of patient information leaflets, RUT/PIL testing and bridging reports, translations and archiving of registration documents.
Consultancy to implement quality management systems, lead-auditor services and accreditation/certification preparation including medical device readiness, pre-inspection audits and CAPA development.
Outsourced pharmacovigilance operations including case intake and processing, regulatory reporting, literature monitoring, PV system audits, inspection support and signal management for marketed products and clinical trials.
Preparation and submission of regulatory dossiers, liaison with competent authorities, MAH support, renewals, variations, labelling and packaging text services across medicinal products, medical devices, food supplements and cosmetics.
Full-service clinical trial support including project management, monitoring, site feasibility and qualification, logistics for investigational products and supplies, patient recruitment support and preparation for regulatory inspections.
Design and management of patient support programmes, including nurse-led education, adherence monitoring and multi-channel patient engagement.
Creation and review of regulatory and promotional documentation, preparation of patient information leaflets, RUT/PIL testing and bridging reports, translations and archiving of registration documents.
Expertise Areas
- Pharmacovigilance and safety surveillance
- Regulatory affairs and product registration (medicinal products, devices, cosmetics, supplements)
- Clinical trial management and site monitoring (Phases I–IV)
- Quality management systems and auditing for healthcare
Key Technologies
- Cloud-based pharmacovigilance case management systems
- Web and mobile-accessible safety databases
- Literature monitoring and signal detection workflows
- eCTD XML backbone and lifecycle submission standards
News & Updates
According to Pharma Tech Outlook, Marti Farm is ranked among the top 10 pharmacovigilance consulting companies in Europe.
Marti Farm received a grant of 300,000 HRK for the project to develop and implement an IT pharmacovigilance solution compliant with ISO IDMP standards.
An article discussing the upcoming trends and changes in pharmacovigilance practices worldwide.
An overview of how the pandemic has affected pharmacovigilance operations and the measures taken by Marti Farm.
Ranked by Pharma Tech Outlook for excellence in pharmacovigilance consulting.
According to Pharma Tech Outlook, Marti Farm is ranked among the top 10 pharmacovigilance consulting companies in Europe.
Marti Farm received a grant of 300,000 HRK for the project to develop and implement an IT pharmacovigilance solution compliant with ISO IDMP standards.
An article discussing the upcoming trends and changes in pharmacovigilance practices worldwide.
An overview of how the pandemic has affected pharmacovigilance operations and the measures taken by Marti Farm.
Ranked by Pharma Tech Outlook for excellence in pharmacovigilance consulting.