Abiogenesis - Leading Clinical Research Organization.
Abiogenesis is a leading ASIA PACIFIC Clinical Research Organization (CRO) Headquartered in Hyderabad, India along with clinical operations staff (PM’s & CRA’s) in Philippines, Tanzania, Thailand, Vietnam, Bangladesh and Middle East supporting the clinical trials including but not limited to drugs, nutraceuticals, medical devices etc innovations to improve the patient healthcare in clinical settings by providing new treatment options and alternatives through clinical strategic development.
We, at Abiogenesis Clinpharm CRO expertise in understanding the project, its unique and succinct clinical development, in which efficiency and accuracy is utmost, is valuable and ambitious to long-term success.
We specialize in clinical trial services including, Oncology, endocrinology, real world evidence, immunology, dermatology, etc. Our reputation in clinical trial services differentiate us from conventional Clinical Research Organization (CRO). We leverage our Scientific leadership to domicile and conserve assurance of unique investigators network for clinical research services.
Explore Our Main Services
Our Clinical Operations Team is experienced in managing clinical trials of varied size and complexity in different therapeutic areas
Our Data Management Team is fully compliant for 21 CFR part 11 and has capability to deliver extensive clinical data management projects
We have a dedicated Quality Assurance Department to ensure that your projects will receive the highest level of quality in on time
Our Medical Affairs Department comprises of physicians, scientific writers and safety experts, And compliance with requirements
Our Biostatistics and Programming Team can manage complex studies by performing in-depth analysis of data in different therapeutic areas
Our Regulatory Affairs Department has competency in handling multiple regulatory activities from clinical trial applications
We Are The TRUSTED EXPERTS
Our team has scientific experience and expertise in clinical trials of drugs, vaccines, biosimilars, medical devices, nutraceuticals, and herbal products. We provide comprehensive services, including: clinical sites and investigators, patient recruitment, safety surveillance, clinical monitoring, site audits, project management, data management and biostatistics. We are committed to carrying out clinical studies efficiently and effectively to meet regulatory guidelines and transform research findings into advanced treatments.
How Abiogenesis Will Help You
The successful execution and completion of Clinical Trial is an enormous task involving clinical trial feasibility, financial support, retention and study design efforts that can take years to complete. It is determined by a unified utility system that includes Medical Writing, Clinical Operations, Clinical Project management, Clinical Data Management, Statistical Analysis, Site Management, Regulatory Affairs, Pharmacovigilance and beyond.
We are dedicated to tailoring the best ethical and clinical practices in the execution of clinical research studies, in addition to patient safety. Our aim is to provide customized clinical project management with accurate and reliable clinical data.
Abiogenesis Clinpharm, CRO is open to all clients to provide suite of clinical trial services
- Project Management
- Clinical Operations
- Regulatory Affairs
- Medical Affairs
- Clinical Data Management
- Quality Assurance
- Biostatistics
- Pharmacovigilance
- FSP
We at Abiogenesis Clinpharm aim to advance clinical trials that enhance patient lives through holistic approaches, focus on patient-centric needs, utilize cutting edge technology and most importantly, abide by stringent safety measures and data management practices. With patient-centric trial designs, increased engagement strategies of patients, focus on ensuring safety and improving diversity with technology solutions in clinical trials, stakeholders can contribute significantly towards better health outcomes.