Site Selection and Feasibility
Site Selection and Feasibility
Site Selection and Feasibility
We assist in identifying optimal clinical trial sites and conduct thorough feasibility assessments, ensuring the right sites are selected for the study.
Regulatory Support
Site Selection and Feasibility
Site Selection and Feasibility
Our team of experts navigates the complex regulatory landscape, providing guidance and ensuring compliance with local and international regulations throughout the trial process.
Study Start-Up Services
Site Selection and Feasibility
Study Start-Up Services
We offer efficient study start-up services, including contract and budget negotiation, ethics committee submissions, and investigator training, to accelerate the initiation of clinical trials.
Data Management and Biostatistics
Data Management and Biostatistics
Data Management and Biostatistics
We employ robust data management systems and employ experienced biostatisticians to ensure accurate data collection, analysis, and reporting.
Project Management
Data Management and Biostatistics
Data Management and Biostatistics
Our dedicated project managers oversee every aspect of the trial, from planning and implementation to monitoring and closeout. They serve as a single point of contact, ensuring effective communication and coordination among all stakeholders.
Quality Assurance and Compliance
Data Management and Biostatistics
Quality Assurance and Compliance
We have stringent quality assurance protocols in place to ensure adherence to Good Clinical Practice (GCP) guidelines and quality standards throughout the trial.
Manuscript and Protocol Writing
Manuscript and Protocol Writing
Manuscript and Protocol Writing
With a team of experienced writers and subject matter experts, we possess the expertise needed to create compelling and well-structured manuscripts and protocols. We are well-versed in the intricacies of academic writing, scientific research, and the specific requirements of various disciplines.
Ethics Committee Registrations
Manuscript and Protocol Writing
Manuscript and Protocol Writing
We have developed a deep expertise in the field of ethics committee registrations. With our dedicated focus and extensive experience.
When it comes to ethics committee registrations, we possess unparalleled knowledge and understanding of the process. Our team of experts has a thorough understanding of the regulatory requirements, ethical
We have developed a deep expertise in the field of ethics committee registrations. With our dedicated focus and extensive experience.
When it comes to ethics committee registrations, we possess unparalleled knowledge and understanding of the process. Our team of experts has a thorough understanding of the regulatory requirements, ethical principles, and best practices involved in establishing and maintaining an ethics committee.
Trainings
Manuscript and Protocol Writing
Trainings
We offer comprehensive GCP/GLP training services to ensure professionals in the pharmaceutical and research industries are equipped with the necessary knowledge and skills to adhere to Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) guidelines.
Clinical Trials
ABSOLUTE RESEARCH is actively engaged in providing site management services of clinical research and acts as a common bridge between the Principal Investigators and Sponsors/CROs for the successful execution of clinical trials (Phase I-IV, BA/BE Studies/Observational Study/Medical Device) across various therapeutic areas. We provide the t
ABSOLUTE RESEARCH is actively engaged in providing site management services of clinical research and acts as a common bridge between the Principal Investigators and Sponsors/CROs for the successful execution of clinical trials (Phase I-IV, BA/BE Studies/Observational Study/Medical Device) across various therapeutic areas. We provide the trained CRC, Experienced Principal investigator, proper constituted institutional Review Board/Institutional Ethics Committee (As per New Drug CT rule 2019) along with data integrity.