E-Merge tech BioPharma Intelligence

Our Bio-Pharma Intelligence Research is a highly value adding service spanning the Entire Life Cycle of Product Development and commercialization. We provide Therapeutic & Scientific Intelligence team with experienced Physicians, Pharmaceutical, Biotech and Medical Diagnostic experts to Assure the Quality in Drug, Device, and Biological Development that can reliably serve the entire Regulatory services with Pharmacovigilance spectrum Our Expertise : Regulatory Strategy & Gap Analysis : We help clients navigate the complex and ever-changing regulatory landscape with ease, from proof-of-concept to product approval. Our approach is to implement regulatory strategies successfully beyond just compliance. Pharmacovigilance & Materiovigilance : We provide evidences that support the various stages such as the collection, detection, assessment, monitoring, and prevention of adverse effects with Pharmaceutical & Medical device products. Medical Writing : We offer a wide range of Medical Writing services, from individual documents to larger Medical Writing projects tailored to our customer's needs. PRISMA Literature Review : Our team ensures the safety is monitored right from the Medical Literature Monitoring (MLM), Clinical Evaluation Report, Global literature (like PUBMED, Embase, Medline, MedDRA, VigiBase) and local literature review in identifying ICSRs, signals and information for inclusion in Periodic Safety Update Reports (PSURs). Meta Analysis : E-Merge tech Meta-Analysis Experts will ensure a thorough review of your Research Studies, conduct an Epidemiological Study design used to Systematic review, Data extraction, Evaluating, and Synthesizing all High-quality Evidence and apply extensive references of Primary Studies relevant to compare similar Research Studies. Dossier / Technical File / CE Marking : We are committed to provide you Compliance and Compatible Dossier / Technical Fie / CE Marking on time with High-quality Deliverables.