Clinical Research Organization, Regulatory, Scientific Writing Services

A  clinical research organization  conducts clinical trials and testing on drugs developed by the  pharmaceutical companies  before they’re introduced into the marketplace for commercial use. Following are the phases of a clinical trial: • Phase 0: small dose of a drug on limited number of in-patients • Phase I: observing the consequences of various drug dosage on a gaggle of 20-40 people to seek out the perfect dosage capacity • Phase II: trial to guage and compare the effect of the new drug as compared to the effect of existing drugs for an equivalent medical condition. This phase is usually administered on a wider scale (~3000 participants) • Phase III: trial after FDA approval of the drugs . It involves thousands of participants and may last for years. Apart from testing for the effectiveness of a drug, a clinical research organization also offers the next services to varied pharma and biotechnological companies:- •  Clinical data management •  Pharmaco...

Regulatory writing services for drugs and medical devices. Pepgra offers global regulatory and  clinical writing services . The team delivers clinical study protocols and findings with precision. Reports are scientifically accurate, culturally sensitive, and meticulously compliant with regulations and statutory bodies. Drugs and Medical Devices  Pepgra Extensive Regulatory Experiences For medical device manufacturers Our Expertise and Experience Our Experts (Regulatory Medical Writers): Therapeutic Areas that we work Editing & Formatting: Our Quality Control & Assurance: Delivery: 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. ...