Clinical Research Organization, Regulatory, Scientific Writing Services

Pharmacovigilance services also are mentioned as drug safety-related services, are the pharmacological science concerning the gathering , discovery, evaluation, monitoring, and prevention of adverse outcomes with pharmaceutical products. As such, pharmacovigilance gradually concentrates on adverse drug reactions, or ADRs, which are described as any response to a drug which is noxious and unintended, including lack of efficacy. Prescription errors like overdose, and misuse and abuse of a drug also as drug exposure during pregnancy and breastfeeding, also are of concern, even without an adverse event, because they'll end in an adverse drug reaction. Ultimately, pharmacovigilance service are concerned with recognizing the danger s linked with pharmaceutical products and with minimizing the danger of any harm which can come to patients. Organizations must lead a comprehensive drug safety and pharmacovigilance audit to assess their compliance with worldwide laws, regulations, and gu...

Pepgra offers pharmacovigilance Literature review search services as a part of the drug safety and efficacy services. Our medical regulatory staff have extensive experience in checking out articles from multiple databases published and may comprehensively manage your literature screening requirement during a cost-effective manner in conjunction with writing periodic safety reports. Our literature specialist team of Pepgra has 15+ years of experience in global pharma, with attention on literature. We work closely with customers on one-on-engagement model and develop the search strategy methodology to make sure that criteria are robust and an unbiased approach. We perform the literature search be for aggregate reports, or benefit-risk analyses or for signal evaluation or ongoing screening as needed by local and regional requirement. Our weekly search isn't only limited to the identification o...