Partnering with Pepgra, CRO can provide strategic benefit
realized as a time and cost saving in the development and approval process of a new therapeutic agent or device
Pepgra works with principles of creativity, value timely deliverance, and more importantly, believe in driving the process proactively. We fulfil the areas where sponsor organization is lacking like personnel strength, technology, facility needed for specific research without actual increase of resources at sponsors end. Our experts are seasoned monitors, trained on the protocols, standard operating procedures, applicable FDA guidelines and good clinical practices.
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

Cost effective

Transparency

Constant Training
Our experience
Pepgra CRO is a team of creative, highly qualified and experienced professionals who are committed to achieving complete client satisfaction through timely quality work. Pepgra ranks high amongst the few full-service contract research outsourcing organizations that include clinical research, clinical monitoring, bioavailability/ bioequivalence and post-marketing study/ surveillance. MedEx possess wide experience in handling a broad spectrum of therapeutic areas since we constantly look out to expand our knowledge database by wanting to conduct trials in many more indications. Vast experience in working across multiple therapeutic areas like Biochemistry, Diabetes, Gastrointestinal, Renal/Nephrology, Respiratory, Psychiatry, Rheumatology, Cardiovascular, Toxicology and Oncology

Overview
Welcome to Pepgra.
Pepgra is a leading global contract research outsourcing organization provider of scientific, knowledge-based services to bio-pharmaceutical, generic pharmaceutical, biotech, medical device companies and healthcare companies in the areas of clinical trial monitoring, regulatory writing, post-market surveillance, biostatistics and statistical programming services. Our mission is to become a strategic partner to global life science companies providing high quality knowledge-based expertise across the product lifecycle with the ultimate objective of improving quality of healthcare for patients worldwide. Our corporate headquarter is located in India with operations in USA, and the Philippines. .
Stepping up
Our distinct combination of scientific expertise, process rigor and technology innovation delivers consistent, reliable and insightful results.
Call us
Our distinct combination of scientific expertise, process rigor and technology innovation delivers consistent, reliable and insightful results.
Fax
Our distinct combination of scientific expertise, process rigor and technology innovation delivers consistent, reliable and insightful results.
The agility to
grow with your needs
Our process, technology solutions and culture of excellence give us the ability to scale up
without compromising on quality
Supporting you
through the entire product lifecycle
From study design to post marketing surveillance and commercialization support.
