Clinical Trial & Contract Research
CLINICAL TRIAL
Our Clinical Trials encompass a broad spectrum, including Anaesthesiology, Emergency Medicine, Medical Surgery, Obstetrics & Gynaecology, Ophthalmology, Oral & Maxillofacial Surgery, Orthopedics, Otorhinolaryngology, Pediatric, Psychiatry, Radiotherapy & Oncology, Rehabilitation, Respiratory Medicine, and Surgery.
These services are supported by a robust infrastructure that includes cutting-edge facilities and equipment. Our research capabilities boast an EEG unit, on-site laboratories, and advanced imaging technologies such as MRI and CT scans. The on-site pharmacy ensures seamless drug management, and our drug storage facilities, including refrigerated centrifuges, freezers at -20 °C, and freezers at -80 °C, adhere to the highest standards.
Drawing from a wealth of clinical trial experiences in Cardiology, Endocrine/Metabolic studies, Haematology, Oncology, and Paediatrics, EHS Clinical Trials bridges the gap between research and clinical expertise, contributing to the advancement of medical science and the enhancement of patient care.
These services are supported by a robust infrastructure that includes cutting-edge facilities and equipment. Our research capabilities boast an EEG unit, on-site laboratories, and advanced imaging technologies such as MRI and CT scans. The on-site pharmacy ensures seamless drug management, and our drug storage facilities, including refrigerated centrifuges, freezers at -20 °C, and freezers at -80 °C, adhere to the highest standards.
Drawing from a wealth of clinical trial experiences in Cardiology, Endocrine/Metabolic studies, Haematology, Oncology, and Paediatrics, EHS Clinical Trials bridges the gap between research and clinical expertise, contributing to the advancement of medical science and the enhancement of patient care.
CONTRACT RESEARCH
Our Contract Research epitomizes excellence in collaborative research endeavors, offering a comprehensive range of services to support pharmaceutical and healthcare industries.
Our dedicated team of experts engages in customized contract research, ensuring the highest standards in study design, execution, and analysis.
1. Preclinical Research: Involve testing the safety and efficacy of potential drug candidates in laboratory settings or on animals before human trials begin.
2. Clinical Trials: Includes recruiting and managing study participants, collecting and analyzing data, and ensuring that trials are conducted in compliance with regulatory requirements.
3. Regulatory Affairs: Assist pharmaceutical companies in navigating complex regulatory processes by helping with the preparation and submission of regulatory documents required for approval.
4. Data Management and Analysis: Specialize in managing and analyzing the vast amounts of data generated during clinical trials. This includes statistical analysis to determine the safety and efficacy of the investigated drugs.
5. Quality Assurance: Ensuring the quality and integrity of the research process is crucial. Dedicated quality assurance teams to monitor and audit processes to comply with industry standards and regulations.
6. Post-Marketing Surveillance: After a drug is approved and on the market, post-marketing surveillance involve to monitor the drug's safety and effectiveness in real-world conditions.
7. Biostatistics: Statistical analysis is a critical component of clinical research. Biostatisticians will analyze and interpret data generated during clinical trials.
Our dedicated team of experts engages in customized contract research, ensuring the highest standards in study design, execution, and analysis.
1. Preclinical Research: Involve testing the safety and efficacy of potential drug candidates in laboratory settings or on animals before human trials begin.
2. Clinical Trials: Includes recruiting and managing study participants, collecting and analyzing data, and ensuring that trials are conducted in compliance with regulatory requirements.
3. Regulatory Affairs: Assist pharmaceutical companies in navigating complex regulatory processes by helping with the preparation and submission of regulatory documents required for approval.
4. Data Management and Analysis: Specialize in managing and analyzing the vast amounts of data generated during clinical trials. This includes statistical analysis to determine the safety and efficacy of the investigated drugs.
5. Quality Assurance: Ensuring the quality and integrity of the research process is crucial. Dedicated quality assurance teams to monitor and audit processes to comply with industry standards and regulations.
6. Post-Marketing Surveillance: After a drug is approved and on the market, post-marketing surveillance involve to monitor the drug's safety and effectiveness in real-world conditions.
7. Biostatistics: Statistical analysis is a critical component of clinical research. Biostatisticians will analyze and interpret data generated during clinical trials.
OUR PORTFOLIOS
Contact Us
For more information or potential collaboration, feel free to reach us at:
Usains Healthcare Sdn Bhd,
USM Kampus Kesihatan
Kubang Kerian, 16150 Kota Bharu, Kelantan
CONTACT PERSON:
Ms. Kasyifah
Pn. Nur Fatin Fatihah
Ms. Kasyifah
Pn. Nur Fatin Fatihah
EMAIL:
kasyifah@usainsgroup.com
uts.fatinfatihah@gmail.com
kasyifah@usainsgroup.com
uts.fatinfatihah@gmail.com
PHONE:
+609-767 3801