Our Services

At Parameters Research Laboratory, we are committed to providing comprehensive and high-quality services to our valued customers. Our key deliverables encompass a range of essential components to ensure the success and integrity of your clinical research projects:

STUDIES

Invasive Blood Pressure

Our team consists of highly skilled medical professionals, including physicians, nurses, and technicians, who are experienced in performing invasive procedures such as arterial catheterization. We have conducted numerous invasive blood pressure studies in various clinical settings and research projects. We utilize the latest technology in arterial catheterization to ensure accurate and reliable measurements of blood pressure and arterial waveforms. We understand that each research or clinical project is unique, and we will work closely with you to develop a study protocol tailored to your specific objectives and requirements.

Non-Invasive Blood Pressure

Whether you are conducting early-phase feasibility studies or large-scale clinical trials, our experienced team can provide end-to-end support. From protocol development to participant recruitment, data collection, and analysis, we ensure that your study is conducted with the highest standards of quality and compliance. Our state-of-the-art equipment and skilled personnel enable us to perform accurate and reliable blood pressure measurements in various test settings.

Human Factors Studies

We conduct human factor studies, also known as human factors engineering or ergonomics, involve the scientific understanding of interactions between humans and other elements of a system. These studies aim to optimize system performance, safety, and user experience by considering human capabilities and limitations. In healthcare settings, human factor studies help optimize and develop equipment design to improve clinical outcomes and patient safety.

IRB Submission

We meticulously handle the Institutional Review Board (IRB) submission process, ensuring that your clinical investigation plans are thoroughly reviewed and approved for ethical considerations.

Regulatory Documents

Our team takes charge of preparing and maintaining all regulatory documents, ensuring compliance with industry standards and guidelines throughout the research lifecycle.

CRFs, ICFs, Health forms

We design and manage Case Report Forms (CRFs), Informed Consent Forms (ICFs), and health forms, streamlining the data collection process and maintaining the highest standards of documentation.

End Point Study Data

We deliver accurate and timely endpoint study data, providing you with valuable insights that are crucial for making informed decisions throughout the research process.

Physical Security

Ensuring the security and integrity of sponsor devices and equipment is a top priority. We implement robust measures to safeguard these essential tools throughout the research duration.

Data Security

Protecting the confidentiality and privacy of participant personal information and client-sensitive data is paramount. Our stringent security protocols ensure that all information is handled with the utmost care and in compliance with data protection regulations.

Get a Quote

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