Clinical Trial Patient Recruitment
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 Trial Patient Recruitment
We streamline your recruitment strategy.
Pepgra patient recruitment team facilitates the recruitment process based on your protocol, pre-screening conditions and inclusion/exclusion criteria. You pay only for the successful enrolment of patients thereby eliminating risk for sites and sponsors. Our team of experts dedicate their time and energy to recruit patients for all clinical trials across the globe. This applies to all therapeutic areas as well.
Comprehensive Patient Recruitment Solutions
Our system locates and provides access to ideal patient populations based on ICD-9 codes and positions your study site for success.
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 Notified Bodies…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.
Pepgra’s processes are on par with Clinical Data Interchange Standards Consortium (CDISC) principles. They ensure thoroughness at each phase and report accurate findings. Face your uncertainties with the help of their statisticians.
— Dave Miller, CEO of leading drug manufacturer
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).
