SYMOGEN is a niche service provider for all aspects of Pharmacovigilance, Pharmacoepidemiology, Medical Writing & Regulatory Services. Established in 2007, our clients are large and midsize pharmaceutical, biotech and medical device companies.
Global Presence
SYMOGEN’s global presence in UK, USA and India allows for the accurate gathering of detailed regulatory intelligence, offering round the clock case processing services in Clinical and Post- marketing arenas, Aggregate reporting services, Labelling services, Signal detection activities and Risk-Benefit report preparations and submission of safety reports to regulatory bodies ensuring a high level of quality and compliance.
More than 10 years of experience providing Pharmacovigilance/Pharmacoepidemiology, Medical Writing and Regulatory services, our team of global experts include highly qualified, trained and experienced professionals from the corporate and academic world.
Quality & Compliance
Our emphasis regarding the provision of PV, Regulatory or any other services focuses on both quality and compliance. Quality is fundamental to the successful operation of any outsourced services, particularly where customer satisfaction is concerned; Compliance in terms of PV, Regulatory services is paramount to adherence to applicable legislation and regulatory time-frames and SYMOGEN staff aim only for 100% in this regard.
Cost Effective and flexible Solution
SYMOGEN offers functional and tailor made services to meet Client’s budgetary requirements efficiently and systematically, emphasising on Flexible and scalable solutions customized to business and technical requirements.