THE ELIXIR FOR THE AILING CRO

We’re the elixir for the ailing CRO. We want to create a paradigm shift in the way the CRO industry works.

We want to create a paradigm shift in the way the CRO industry works.

Our goal is to delight our customers, and execute your project flawlessly. We continually seek improvements and aim to not just successfully close your trial, but surpass your expectations. Our goal is to realize your ambitions.

WHAT MAKES PEPGRA UNIQUE?

Flexibility & adaptability

Pepgra is flexible and adapts according to your project’s changing requirements. That is why we allocate a relationship manager.

Standards & Compliance

We follow stringent guidelines and 100% compliance with FDA, EU, and ICH standards. Certified by AMWA and EMWA.

Global footprint

Our medical and native gurus are located in more than 60 countries; we know your regulatory requirements, ethics, protocols and standard practices.

YOU’RE RELIABLE CRO PARTNER

We’re the elixir for the ailing CRO. 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.

Our goal is to delight our customers, and execute your project flawlessly. We continually seek improvements and aim to not just successfully close your trial, but surpass your expectations. Our goal is to help you script a successful clinical research trial. We want to create a paradigm shift in the way the CRO industry works. Pepgra's uniqueness is contractual flexibility, relationship and expertise in niche areas.

CERTIFIED WRITERS

Our writers have these qualifications: MD, MBBS, PharmD, and PhD. In addition, they are knowledgeable in regulatory protocols of more than 100 countries. Our medical writers hold experience in handling a wide range of therapeutic areas and all phases of development.

BIOSTATISTICAL PROGRAMMING

Pepgra offers regulatory biostatistical analysis as per the principles outlined in the International Conference on Harmonization (ICH) E9 guidelines. We bring a deep understanding of the science of disease and compounds—comprehensive planning assistance.

POST-MARKET SURVEILLANCE

Pepgra will help you maintain compliance. Our PMS experts will help you stay on track and succeed through audits and reviews done by regulatory authorities. By taking your PMS seriously you will never be in the bad books of the law.