Hybrid Approach Clinical Development Involves therapeutic realignment
and native research scientists
to build the best monitoring
team for you
Patient Performance Drug Monitoring Plethora of expertise in monitoring
drug and patient performance
during trials.
Dedicated Solutions All Specializations Experience in conducting multiple
trials and we want to share our
insights
SEAMLESS CLINICAL SUPPORT TO ENHANCE
PATIENT EXPERIENCE.
Pepgra has plethora of experience in conducting clinical
research trials. Let our experts call the shots.
Request Proposal
Protocol Adherence Certified Writers We have professionals (PhDs) in
pharma, medicine, life sciences,
and biotechnology
Data Analysis Medical Statistics Our charts, statistics, analysis and
design will help you make
decisions in a jiffy.
Dedicated Solutions All Specializations Experience in conducting multiple
trials and we want to share our
insights
REGULATORY WRITING: A PIVOTAL FACET OF RESEARCH Pepgra writers are certified by American Medical Writers association
(AMWA) and European Medical Writers Association (EMWA).
A stickler when it’s about adherence to protocols
such as: ICH, FDA, EU and GCP
Request Proposal
Protocol Adherence Certified Writers We have professionals (PhDs) in
pharma, medicine, life sciences,
and biotechnology
Data Analysis Medical Statistics Our charts, statistics, analysis and
design will help you make
decisions in a jiffy.
Dedicated Solutions All Specializations Experience in conducting multiple
trials and we want to share our
insights
THERAPEUTIC EXPERTISE PAR EXCELLENCE Wondering whom to choose? Don’t bat an eye lid because
Pepgra is your ally when it comes to therapeutics.
Our know-how will make your job easier
Request Proposal
Hybrid Approach Clinical Development Involves therapeutic realignment
and native research scientists
to build the best monitoring
team for you
Patient Performance Drug Monitoring Plethora of expertise in monitoring
drug and patient performance
during trials.
Dedicated Solutions All Specializations Experience in conducting multiple
trials and we want to share our
insights
NAVIGATE RIGORS OF MONITORING WITH FLAIR It may seem daunting at first, but rest assured;
leave the task of medical monitoring to us.
Request Proposal
Hybrid Approach Clinical Development Involves therapeutic realignment
and native research scientists
to build the best monitoring
team for you
Patient Performance Drug Monitoring Plethora of expertise in monitoring
drug and patient performance
during trials.
Dedicated Solutions All Specializations Experience in conducting multiple
trials and we want to share our
insights
BIOSTATISTICS FOR DECISIVE DECISION MAKING Scrambling for data and information? Mission critical
scenarios deem decisive decisions from the top helm.
Pepgra will give you the numbers to make
prudent decisions
Request Proposal

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

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

Cost effective


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

Transparency


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

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.