eCTD Publishing Services
At RegConsult, we understand the intricacies and demands of eCTD submissions in the pharmaceutical and healthcare industries. Our expert team is dedicated to ensuring your… Read More »eCTD Publishing Services
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End-to-end Labelling with our fully-managed service
The journey starts here… Just like your medical products, their associated labelling enters on a similar regulatory journey – from the earliest stages of development,… Read More »End-to-end Labelling with our fully-managed service
Medical Product Lifecycle Support
Navigating Regulatory Landscapes Successfully managing a medical product’s lifecycle requires more than just compliance; it demands strategic foresight. Our service ensures your products thrive in… Read More »Medical Product Lifecycle Support
Regulatory Affairs Outsourcing
Why outsourcing your regulatory affairs is the smart move Competing priorities, a lack of a particular specialism and resource or budget constraints are just a… Read More »Regulatory Affairs Outsourcing
Automating Your Regulatory Intelligence
Stay ahead of the regulatory game Gathering the latest regulatory industry insights to help you keep up-to-date with the ever-changing regulatory landscape is a vital… Read More »Automating Your Regulatory Intelligence
Developing Winning Regulatory Affairs Strategies
The importance of a great regulatory strategy Every regulatory project requires you to have a good regulatory strategy in place to ensure you deliver and… Read More »Developing Winning Regulatory Affairs Strategies
AI in Pharma: Transforming Medical Information and Pharmacovigilance
Exploring the Impact of AI (Artificial Intelligence) on the Pharmaceutical Industry Nicholas Wells, Regulatory Consultant, RegConsult.co This article explores the transformative role of AI in… Read More »AI in Pharma: Transforming Medical Information and Pharmacovigilance
What is Regulatory Affairs? A Comprehensive Guide.
Ensuring Safe and Effective Healthcare Products – If you are involved in healthcare products then the question “What is regulatory affairs?” would most likely have… Read More »What is Regulatory Affairs? A Comprehensive Guide.
Social Listening for Pharmacovigilance in Europe: Where are we in 2021?
Introduction Pharmacovigilance is the obligation for Marketing Authorisation (MA) holders to monitor the safety of their bio-pharmaceutical products throughout their lifecycle. Abreviated to (PV) pharmacovigilance… Read More »Social Listening for Pharmacovigilance in Europe: Where are we in 2021?