Our goal is to delight our customers, and deliver a seamless experience. We continually seek improvements. We aim to not just successfully close your trial, but surpass your expectations. Here are the reasons that lend credence to our credibility as a leading CRO provider

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.

Medical and scientific publications

We have a team of more than 200 professionals, experienced editors in scientific, technical, and medical publications (popularly known as STM) who craft research documents, manuals, and manuscripts in more than 170 specializations in each of those fields. We ensure your documents are prepared according to industry standards and ready for publication. We have an experienced panel of experts who are certified and benchmarked according to industry and regulatory standards that vary in different countries.

Pepgra provides unparalleled flexibility with unlimited editing service levels in both UK and US English. Journal formatting is applicable based on the level of editing that you choose, and a journal pre-check is included based on your request at every stage of the Service Level Agreement (SLA).

Therapeutic focus – A holistic approach

Pepgra follow a holistic approach for all clients from clinical to brand development through all its service offerings. We will stick with you through the complete life-cycle of the service, right from clinical trials to pre-launch, launch, post-launch and finally maturity. Our team has vast experience in handling clinical research projects. We also ensure a perfect finishing touch the end of the service draws near. A fully-equipped, talented and dedicated team of professionals qualified in medicine and creative communication across all therapeutic areas in addition to digital/multimedia specialists, graphic designers, and visualizers.

Global footprint

We have Subject Matter Experts (SMEs) in niche areas to ensure that you script a successful clinical trial story. Our medical and native gurus are located in more than 60 countries; we know your regulatory requirements, ethics, protocols and standard practices.

Flexibility and adaptability

Pepgra is flexible and adapts according to your project’s changing requirements. That is why we allocate a relationship manager with whom you will have constant touch to ensure your project is moving seamlessly. Unlike other providers, Pepgra will make the necessary course corrections whenever the scope of your project changes.

Standards & Compliance

All Pepgra writers are certified by American Medical Writers association (AMWA) and European Medical Writing Association (EMWA). We follow stringent guidelines and 100% compliance with FDA, EU, and ICH standards. All prospective customers do have the option to talk to our experts before starting the project.

Pharma and medical device manufacturers

Our service extends to all the medical device manufactures and pharmaceutical companies across North America and specifically European manufactures. We have a panel of doctors working with us to carry out clinical trials, medical writing and patient monitoring services. We combine novelty and the premium technology in the market to meet our customer requirements coupled with best practices in the industry.