Vibha Sharma
Senior Writer
Latest From Vibha Sharma
Netherlands Pilots New Scientific Advice Service For Clinical Trials
The Netherlands’ Central Committee on Research Involving Human Subjects is gauging sponsor demand for a new scientific advice service for clinical trials, which is for now free of charge.
Netherlands Pilots New Scientific Advice Service For Clinical Trials
The Netherlands’ Central Committee on Research Involving Human Subjects is gauging sponsor demand for a new scientific advice service for clinical trials which is for now free of charge.
Global Pharma Guidance Tracker – April 2024
Stay up to date on regulatory guidelines from around the world with the Pink Sheet's Guidance Tracker. The complete Global Pharma Guidance Tracker, with sortable and searchable listings going back to 2014, is available online.
Global Medtech Guidance Tracker: April 2024
Stay current on regulatory guidelines from around the world with Medtech Insight's Guidance Tracker. Thirty-five documents have been posted on the tracker since its last update.
UK MHRA Considers New Approach To Support Sponsors Throughout Clinical Trial Lifecycle
The UK regulator says it wants to come an ‘enabler’ of clinical trials by helping sponsors to deal with potential problems earlier on in the process.
EMA Pilots Partnering With Companies To Gain Efficiencies In Preparing Drug Assessment Reports
The European Medicines Agency is looking to increase the review efficiency and consistency of its assessors by experimenting with a US FDA-style approach in which companies can voluntarily submit certain information in advance to facilitate the product’s review.