Your Trusted Partner in Clinical Trials
Precision is not just our name; it’s our commitment. We deliver high-quality data and on-time results, ensuring every phase of your clinical trial is executed with precision—from meticulous data entry to proactive issue resolution, and streamlined contract management. Our expertise guarantees that your milestones are met with accuracy and agility.
How do we do it?
Precision Research Management (PRM) enriches your clinical trial process by:
Supplying experienced,
GCP-trained personnel
Each member of our team brings a wealth of industry experience and is rigorously trained in Good Clinical Practice (GCP), ensuring the highest standard of conduct and the integrity of your clinical trial results.
Reducing overhead and ensuring protocol compliance
We streamline your clinical operations, significantly reducing overhead while meticulously adhering to protocol compliance, so you can allocate resources where they’re needed most.
Rigorous quality
assurance
Adherence to strict quality assurance measures is at the core of our operations, guaranteeing that every aspect of the clinical trial meets the industry’s most stringent standards.
Meeting timelines and handling updates
Our proactive approach to project management ensures that we meet critical timelines and efficiently handle any necessary updates, keeping your trial on track every step of the way.
Revolutionize Your Clinical Trial Journey in Croatia
Transform your clinical trial experience in Croatia with Precision Research Management. Discover the advantages of expedited patient recruitment and heightened success rates, enhanced by our effective retention strategies. Benefit from our streamlined coordination for optimal efficiency, comprehensive regulatory compliance, and expert risk management. Experience better responsiveness and superior query management, backed by our deep industry knowledge.
Areas of Practice
At the heart of every clinical trial are data integrity and optimized workflows. We excel in precise eCRF data capture and elevate the significance of your research outcomes. Our tailored management solutions are designed to streamline contract negotiations, accelerating the commencement of your trials. Moreover, we implement innovative recruitment strategies to ensure timely participant enrollment.
Partner with us to transform your clinical trials into paragons of speed, efficiency, and effectiveness.
Years of Expertise & Professionalism in Clinical Research
With a management team deeply rooted in the CRO and SMO industries, we bring a wealth of expertise to every clinical study. Our study coordinators are not only experienced medical professionals but are also specialized experts, often focusing intensely on single disciplines, to provide the most informed and dedicated support possible. Our breadth of experience spans various medical fields, allowing us to craft tailored solutions for a diverse range of clinical research needs. We’re committed to driving excellence in every aspect of our work, ensuring that your research is in the hands of experts.
Our guiding principles
These are the core values of Precision Research Management
01
Precision and Quality
At Precision Research Management, we live up to our name by ensuring every aspect of the clinical trials we manage is executed with meticulous attention to detail and the highest quality standards. We believe in the importance of accuracy in every task, from data collection to patient care.
02
Efficiency and Innovation
We’re dedicated to making the clinical trial process as efficient as possible, leveraging innovative solutions to streamline operations, optimize resources, and deliver results promptly. We’re continually exploring new methods and technologies to improve our services and drive successful outcomes.
03
Ethics and Integrity
We hold ourselves to the highest ethical standards, ensuring that all trials are conducted in compliance with Good Clinical Practice guidelines and all relevant regulations. We respect and prioritize patient safety and confidentiality, and we approach every project with honesty, transparency, and integrity.
General information about SMOs
Services Offered
What services does your SMO provide?
An SMO, or Site Management Organization, specializes in managing clinical research sites and ensuring that the trials conducted at these sites run smoothly. SMOs provide administrative and clinical support to healthcare professionals, allowing them to focus on patient care and data collection while the SMO handles the operational aspects of the study. This includes tasks like regulatory compliance, patient recruitment, data management, and quality control.
How can your SMO improve the efficiency of clinical trials?
While an SMO focuses primarily on the operational management of research sites, a CRO offers a broader range of services that can encompass the entire spectrum of clinical trial activities. This includes designing the study, preparing regulatory submissions, monitoring the trial, data analysis, and reporting the results. CROs may manage multiple aspects of clinical trials across various sites and often provide strategic management services, whereas SMOs are typically more focused on the practical and logistical side of site management
Partnership Queries
How can we partner with your SMO?
Partnering with our SMO is a straightforward process aimed at integrating our expertise with your clinical trial needs seamlessly. Begin by reaching out to us via our contact form, email, or phone number listed on our website. We will schedule a consultation to understand your specific requirements, discuss potential strategies, and outline how our services can align with your objectives. Once we establish a mutual agreement, we will draft a contract detailing the scope of our collaboration, timelines, and responsibilities. Our goal is to ensure that the partnership is tailored to enhance your clinical research efforts effectively.
What are the benefits of partnering with your SMO for our clinical trials?
Partnering with our SMO brings a multitude of benefits to your clinical trials, including:
Expertise: Access to a team of seasoned professionals with specialized knowledge in various therapeutic areas.
Efficiency: Streamlined processes that enhance the speed and efficiency of trial operations, from patient enrollment to data reporting.
Compliance: Assurance of adherence to regulatory guidelines and Good Clinical Practice (GCP), reducing the risk of non-compliance.
Focus: Ability for your clinicians to concentrate on patient care and trial outcomes, as we handle the administrative and operational burdens.
Cost-Effectiveness: Reduced operational costs through efficient resource management and process optimization.
Quality Data: Improved data quality through meticulous monitoring and management, ensuring robust and reliable trial results.
Scalability: Flexibility to scale your trials up or down without the need to invest in permanent infrastructure or personnel.
Our partnership is designed to foster a collaborative environment where your clinical trials can thrive, backed by our commitment to excellence and your research objectives.
Operational Questions
How does your SMO handle data management and confidentiality?
Our SMO treats data management and confidentiality as top priorities. We employ a stringent data governance framework that encompasses secure data collection, storage, and transfer processes compliant with industry standards and regulations, including HIPAA and GDPR where applicable. All clinical trial data are handled through secure electronic data capture (EDC) systems with robust encryption protocols. Access to sensitive data is restricted to authorized personnel only, and we conduct regular training to ensure all team members understand their role in maintaining data integrity and confidentiality. Audits and data integrity checks are routinely performed to prevent and detect any unauthorized access or data breaches.
What measures do you take to ensure compliance with GCP and other regulations?
Compliance with Good Clinical Practice (GCP) and other regulatory requirements is integral to our operations. We maintain compliance by:
- Ensuring all staff are thoroughly trained in GCP and understand the regulatory landscape of clinical research.
- Conducting our processes in line with the International Council for Harmonisation (ICH) guidelines.
- Keeping up-to-date with changes in regulations and updating our procedures accordingly.
- Implementing comprehensive standard operating procedures (SOPs) that are regularly reviewed and audited.
- Collaborating closely with ethics committees and regulatory bodies to ensure all aspects of our clinical trials are transparent and compliant.
- Engaging in regular internal and external audits to monitor compliance and promptly address any areas for improvement.
Study Coordinator Specifics
What qualifications do your study coordinators have?
Our study coordinators are highly qualified professionals with extensive backgrounds in clinical research. They typically hold degrees in life sciences, nursing, or related healthcare fields. In addition to their academic credentials, they have also completed comprehensive training in Good Clinical Practice (GCP) and are well-versed in regulatory compliance, patient care, data management, and trial protocols. Continuous professional development is a cornerstone of our practice, ensuring that our coordinators stay at the forefront of clinical research trends, technology, and regulations.
Can we choose a study coordinator specialized in a specific therapeutic area?
Absolutely. We understand the importance of specialized knowledge in conducting successful clinical trials. Our diverse team includes study coordinators with expertise across various therapeutic areas.During the partnership initiation, we will discuss your specific needs and provide you with profiles of coordinators who have the expertise in the therapeutic area of your trial. This allows you to choose a study coordinator whose experience aligns closely with your project’s focus, ensuring the highest level of insight and oversight.
Hours
Mon – Fri
9:00 am — 5:00 pm
—
Contact
Phone
+385 99 4277 865