2GL Outsourcing provides a comprehensive and flexible solutions for the active management of drug safety, pharmacovigilance and risk management during the complete lifecycle of a medicinal product. We offer you a Qualified Person Responsible for Pharmacovigilance (QPPV) services, which includes having an overview of the safety profiles and any safety concerns in relation to the medicinal products and reporting of adverse reactions related to them, both locally and worldwide. We as well keep up with latest literature information regarding adverse events, writing of Periodic Safety Update Reports (PSURs), communicating with Regulatory Authorities and so on.
We offer comprehensive support across all phases of clinical development
We have the experience in training staff for both Sponsors and Investigators
We have highly trained, qualified and experienced research nurses.
We offer this service to the Sponsors and Clinical Research Organizations (CROs).
We offer services that can reduce the registration process and obtaining a drug license for our clients.
We provide a clinical trial related services to our clients.
We provide a clinical trial related services to our clients.
We are looking for freelancers