Clinical Technology & Process
Services
- Clinical Trial Audit & Monitoring
- Clinical Study Design
- Global Regulatory & Clinical Writing
- Clinical Biostatistics
- Clinical Trial Patient Recruitment
- Regulatory Affairs
- Clinical Data Management
- Post-Market Surveillance
- Clinical Technology & Process
- Healthcare Analytics
- Global and Local Literature Search Screening
Clinical Technology & Process
Due to an enormous degree of technological innovation in the healthcare system, today’s hospitals have become technologically sophisticated centres of healthcare delivery and thus demand technologically competent staff
Pepgra CRO offers clinical technologists with the technology side of clinical operations where they play an important role in assisting the hospitals or physicians by providing the technological support they require.
Pepgra CRO offers you the state of the art services in clinical technology. Our long experience with Electronic Data Capture technology in clinical procedures has enabled us to become one of the frontrunners in clinical technology services industry. We serve biotechnology, medical device, and pharmaceutical companies with technological support to manage their clinical R & D trials, technology infrastructure, and business operations.
Our global delivery model provides native language support and multilingual support to serve your patients, investigators, site staff, and supervisors. We offer complete assistance in site assessment and internet service provider connectivity. We evaluate technological infrastructure of the site and ramp-up requirements that would facilitate access to clinical applications and facilities. With our in-house expertise, we ensure that your sites are equipped with custom software images. We provide the necessary hardware support besides solutions for breakage, warranty repairs, and sophisticated remote diagnosis devices to monitor the end-users in the trial.
Our close-out process has been so designed that the data delivered is highly secure and in time. Besides, the process has provision for quality assurance and confirmation from the investigators once they have received and reviewed it. Having understood the varying needs and preferences of our clients, we provide maximum flexibility and scalability to realize their enterprise goals. We leverage our in-house expertise in Life Sciences Support Service to provide the most cost-effective and high-quality service to our clients. Our assistance to pharmaceutical companies in upgrading their IT infrastructure has helped us understand the interaction between the pharmaceutical industry and IT in the global organization and upscale our service offering for Life Sciences Clients.
Our clinical technology training module, which is offered by our experts in-person or through the web, intends to develop your software skills and business process knowledge to help you obtain more accurate and comprehensive clinical trial data. We recognize the challenges before the sponsors and service providers. We are committed to establishing and developing sustainable contracts and working towards achieving a strong partnership with our clients.
Comprehensive Clinical Technology & Process Solutions
Our services include
Other services include biostatistical services overview, drug strategy analysis, drug accountability and reconciliation overview, interactive response technology, investigator selection, trial site initiation, patient recruitment, application support, provisioning, site assessment, data integration, electronic clinical outcome assessments, electronic clinical outcome assessments features and electronic clinical outcome assessment reporting
Brochure
Biostatistical capabilities
We give solutions to the healthcare, pharmaceuticals and food industries to boost sophistication of statistical elements in their study…. Read More
White Paper
Clinical evaluations
Clinical Evaluation Report (CER) in a more Stringent Regulatory Environment- Now, subject to more intense scrutiny by Noti¬fied Bodies…Big Data in IoT for Healthcare Read More
Blog
Medical writing
The requirements for medical writing are witnessing continuous growth influenced in good portion by the mounting government scrutiny and… Read MorePepgra has done plethora of work in the area of clinical data management for top pharmaceutical and medical device companies. All our experts comply with international regulatory standards and protocols—in all phases of development.
We deliver study designs balanced to meet your business needs and expectations with the current scientific understanding and all regulatory requirements considered.
Allow us to help propel your product forward.
The Boston Biomedical Associates team was instrumental in their support of AtriCure in executing our ABLATE trial, interacting with the FDA and preparing for the panel meeting. We are impressed with their extensive clinical and regulatory expertise as well as their professionalism and appreciate their support in working with us to achieve a positive panel vote.
— David J. Drachman, Former President and Chief Executive Officer of AtriCure, Inc.
We’ll scale
up as your needs grow.
No compromising on integrity and quality. Our processes are well defined and flexible to ramp up as per your requirements.
Partnering with
you till the project end.
We come with you all the way. From design to market support
Pepgra CRO Offerings
"Changing global regulatory system, globalization of clinical trials, increased consumer expectations, infrastructural and culture issues, and various diagnostic requirements should never hamper your research and development programs. With our support..."
Download brochure on our CRO offerings (PDF).
