Search Results for: "Category: Pharmacovigilance"

In today’s life sciences industry, many pharma and biotech companies hire outside vendors to help meet business needs, and this assistance is especially critical during regulatory inspections. Quality and communication…

Aggregate reports provide periodic review of safety data in a global and cumulative way. The process requires the collection and assessment of safety data as well as handling the necessary…

Med Communications provides high-quality pharmacovigilance support to our clients to ensure that all individual case safety reports (ICSRs) are processed in a timely and accurate manner. Our well-established, automated workflow…

Med Communications’ team of highly skilled pharmacovigilance (PV) professionals bring practical experience and diverse perspectives to the table. Each of our specialists has a background in medicine, pharmacy, or another…

Med Communications offers a boutique pharmacovigilance experience with global reach, combining personalized attention with international regulatory expertise. Seamless integration of pharmacovigilance and medical information improves workflow efficiency. Our approach combines innovation…

A pharmacovigilance (PV) system covering all PV activities is required of all marketing authorization holders. This system must include the activities of collection and processing of safety information, reporting to…

Every clinical trial requires safety monitoring and management, beginning early in the product development life cycle. The data obtained during safety monitoring help with product safety profile classification and also…

Pharmaceutical companies operate in a highly regulated environment, especially when it comes to global pharmacovigilance (PV) systems. Pharmacovigilance professionals play a crucial role in protecting patient safety while navigating complex…