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Managing trials in various regions is challenging and requires local knowledge and know-how, which is one of Optimapharm’s key strengths.Read More
With country based regulatory specialists and experienced Country Managers, Optimapharm’s regulatory team understand the nuances and complexities of each country’s regulatory demands and processes, therefore extremely capable to expedite the start-up of clinical projects across Europe whilst accessing some of most dynamic recruitment regions in Europe.
The monitor is the client’s contact with site and we cherish that relationship within Optimapharm.Read More
Optimapharm is proud to have monitors with university degrees, predominantly in medical and life sciences. On average, our monitors have more than 5 years of experience in monitoring and adopt a pragmatic, yet disciplined approach at sites to truly support the Investigators and nursing teams.
It’s all about the safety of patients and we, at Optimapharm , take a patient-centric approach to our trials, thereby facilitating recruitment and reducing the number of withdrawals, whilst ensuring our sponsors requirements are fully met.
The high-quality supervision of a project is amongst the most important factors in delivering success.Read More
Optimapharm has certified Project Managers with experience in managing cross functional teams, ensuring that trials Key Performance Indicators (KPIs) and milestones are met. With an average recruitment rate of 108% of recruitment target, we can guarantee success with our “know-how”.
Data Management is a key element of any clinical trial, especially with the new GDPR guidelines that governs how data must be managed across the whole of Europe. Appropriate data management is critical in providing valuable and solid data to Regulators.Read More
Optimapharm provides you with comprehensive clinical data management services for clinical development.
Statistics play a crucial role in clinical trials and in the drug development process, from trial design to protocol development. Having a fundamental understanding of statistical issues can uphold the integrity of a clinical trial and improve communication between clinicians and statisticians. Through our partnering network we can provide access to some of the leading experts in biostatistics.Read More
The success of Medical writing in clinical research depends upon the proper documentation and the exactness of the research, its planning and results. Optimapharm offers flexible solutions, working with experienced medical writers in various therapeutic areas.Read More
It’s all about the safety of patients and we, at Optimapharm, take care of both patients and product, both the key values for our clients.Read More