Preferred Partner for Advanced Pharmaceutical Research
SpinoS –Indian based Clinical Research Organization which supports sponsors of pharmaceutical and medical device trials as well as other CROs in the following areas of clinical research:
Clinical Trial Planning
SpinoS has over a decade of experience in the planning and designing of translational studies and Phase I-IV Clinical Trials. Our services include:
Our Process
SpinoS can offer a full CRO services which can be contracted individually or as a combined package based on the requirements of each specific clinical project.
Spinos Life Science and Research Private Limited
SpinoS was established with an aim to build a full-fledged CRO offering end to end service with respect to the phase studies, with system and process in compliance with global regulatory standards.
Clinical Trial Management
Our trial managers have extensive experience in setting up, budgeting and conducting phase I to phase IV clinical trials.
Clinical Trial Monitoring
SpinoS has specialized in the monitoring of clinical trials, Functioning as the key communication link between the sponsor and the clinical trial management team, our highly qualified and experienced clinical trial monitors provide excellent service. Our services include:
Our Process
Over the years, we have developed excellent professional relationships with key thought leaders in common research indications such as oncology, cardiovascular disease and CNS. This has proven valuable to sponsors of clinical trials, especially in critical situations, when drawing on these relationships has helped spur recruitment, thus allowing important study timelines to be met
Spinos Life Science and Research Private Limited
SpinoS was established with an aim to build a full-fledge CRO offering end to end service with respect the phase studies, with system and process in compliance with global regulatory standards.
Clinical Site Management
The CRA is the key communication link between the sponsor and the clinical site and is responsible for assisting the site throughout the operative phase of the study to ensure that the trial site has the necessary information and support to conduct the trial according to protocol specifications.Our services include:
Clinical Trial Oversight
Our experienced clinical team performs quality oversight visits for CRO and pharmaceutical clients to review CRA and site performance, assess the qualification of investigators, inspect site documentation and examine drug accounting.
Clinical Trial Documentation
SpinoS documentation experts are able to assist the sponsor in the following areas. SpinoS provides full study documentation support for its clients, Our services include:
Our Process
Over the years, we have developed excellent professional relationships with key thought leaders in common research indications such as oncology, cardiovascular disease and CNS. This has proven valuable to sponsors of clinical trials, especially in critical situations, when drawing on these relationships has helped spur recruitment, thus allowing important study timelines to be met
Spinos Life Science and Research Private Limited
SpinoS was established with an aim to build a full-fledge CRO offering end to end service with respect the phase studies, with system and process in compliance with global regulatory standards.
Drug Supply Management
For each trial it is crucial that the investigational product is properly managed throughout its life cycle from release to destruction.Our Pharmacist ensure that the IP has been manufactured and checked in accordance with internationally accepted standards of GMP for medicinal products for human use, track and guarantee the timely delivery of the IP at the investigational site(s) throughout the trial and assist the CRA and investigational site in all aspects of drug accountability.
Our Process
Our Pharmacist ensure that the IP has been manufactured and checked in accordance with internationally accepted standards of GMP for medicinal products for human use, track and guarantee the timely delivery of the IP at the investigational site(s) throughout the trial and assist the CRA and investigational site in all aspects of drug accountability.
Bio-sample Management
The proper handling, shipment and tracking of biological samples plays a crucial role in many clinical trials. Our Bio-sample Management professionals are experts in this field.
Spinos Life Science and Research Private Limited
SpinoS was established with an aim to build a full-fledge CRO offering end to end service with respect the phase studies, with system and process in compliance with global regulatory standards.
Submissions to EC and Local Authorities
SpinoS has broad experience with the initial and subsequent submission of documents to ethics commissions as well as the registering and cancellation of investigational sites. With our detailed knowledge of all local regulatory and ethical requirements we can provide you the complete submission package or partial service.
Full Service
Its mission is to combine a unique set of clinical research expertise to provide complete service solutions across all stages of the clinical development process from phase I to IV trials as well as retrospective studies. SpinoS can offers to its clients a full range of CRO service, from study setup and conduct, CRF design, data handling, analysis and reporting as well as all aspects of drug safety.SpinoS offers its clients the following services:
☆ Scientific Consulting
☆ Site Selection & Feasibility
☆ Patient Recruitment
☆ Regulatory Services & Provision of Legal Representative
☆ Study Management
☆ Study Monitoring
☆ Study Documentation
☆ Project Management
☆ Data Management
☆ Patient Recruitment
☆ Biostatistics
☆ Medical Writing
☆ Proofreading & Translation
☆ Pharmacovigilance
☆ Safety Writing
