Pepgra is an ISO 9001:2015 certified organization offering comprehensive CRO services. A clinical Research organization (CRO) that provides support to pharmaceutical, biotechnology, and medical device industries in the form of research services outsourced on a contract basis. The company offers clinical trial management support, patient recruitment, regulatory writing, medicine and disease coding, biostatistics, data management & overall project management for drugs and/or medical devices. Our team comprises certified writers, biostatisticians, Clinical Research Associates (CRAs), and therapeutic specialists. We are on par with industry standards and regulations—general demands and institutional demands. Meticulousness in compliance is our credo. FDA, NIH, CDC, HIPAA, and EU protocols (ICH-GCP: R2)—these are some of the regulations we comply with albeit we have not mentioned an exhaustive list of protocols and standards here; moreover, guidelines vary in every country and this is exactly where our CRO connoisseurs contribute— We have traversed all clinical research phases and therefore guarantee you our steadfast support. Here are the reasons that lend credence to our capabilities in customization:• First, we're hands-on (native protocols, regulations, and standards) in conducting all phases of clinical trials & epidemiological research across EU, US, & Asia.• Second, we're abreast with the latest market intelligence through our access to a vast scientific database; yes, our experts are continually updating their skills. Furthermore, we participate in CRO conferences and medical seminars to know the pulse of the regulatory market.• Finally, we attribute our success in customizations to our competent team; Contact us atUK: +44-1143520021US/Canada: +1-972-502-9262India: +91 9884350006https://www.pepgra.com/Download Brochure: https://www.pepgra.com/wp-content/uploads/2018/05/Pepgra_CRO_Brochure_Final.pdfFor Sales: info@pepgra.com I sales.cro@pepgra.com