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

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Biostatistics & Clinical Data Management

Database design & Build, data entry & Validation, medicine & disease coding, statistical analysis plans and reports, validation programming,

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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.

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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

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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
pepgra Constant-Training

Familiarity

familiarity of local regulations and network. Easier to find the right site, investigator and team set up. Patient population and how to assists recruiting
pepgra Cost-effective

Cost effective

Culturally sensitive to the locale and competitive price. Timely delivery of the highest standard of quality
pepgra Transparency

Transparency

All our clinical development services are done in accordance with our SOPs compliant standards & certified by ISO /IEC 27001:2013.
pepgra Constant-Training

Constant Training

Our writers undergo regular training conducted by the AMWA and the EMWA and other recognized medical writing organization to keep their skills at.

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.