Clinical Research / Field Monitoring
we use a hybrid approach of therapeutic realignment and regionally based clinical research associates to build the best monitoring team for each study
Biostatistics & Clinical Data Management
Database design & Build, data entry & Validation, medicine & disease coding, statistical analysis plans and reports, validation programming,
Clinical Regulatory Writing
Our expertise in the area of Regulatory Writing include Medical Devices, Prescription Drugs (with extensive knowledge of pharmacokinetics, pharmacodynamics, pharmacogenomics), Over-the-counter Medicines, Veterinary medicines, Cosmetics, Biologics and Nutraceuticals.
Regulatory Affairs & Consultation
We deliver unparalleled expertise. We act as your liaison in all interactions with regulatory agencies from regulatory strategies to providing regulatory submission support to achieve your marketing objectives
Why outsource to Pepgra CRO
Our size and niche focus on clinical research monitoring, biostatistics, data management, project management, a scientific writing and regulatory report writing enable Pepgra to be more flexible, affordable and scalable. We combine novelty and the premium technology in the market to meet our customer requirements coupled with best practices in the industry
Familiarity
Cost effective
Transparency
Constant Training
Our experience
At Pepgra we are open to new ideas, different people and various cultures. We’d love to hear as to what you can offer us and we’d like to reciprocate as well. People with ideas, skills and qualifications in the medical and pharmaceutical industry are welcome to contact us for any kind of CRO engagements. Pepgra has plenty of skills to offer you in various phases of clinical research trials. Be it regulatory writing, biostatistics, regulatory approvals, trial monitoring, drug/device development, and clinical reports. Our native experts know your market, ethics, protocols and culture. Pepgra is your reliable CRO ally who can pitch in when it is critical. Become our partner today.