Heidi Jerman

7 min read

Top 10 Clinical Data Management Service Providers Transforming Trials in 2025

The clinical research landscape is rapidly evolving, placing increased importance on robust and compliant clinical data management services (CDMS). Effective clinical data management is fundamental to ensuring the quality, integrity, and timely...

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2 min read

Appropriate, early planning for medical device development could help outshine the darkness of Alzheimer’s disease

Exciting developments in the area of medical devices for the diagnosis, prognosis, treatment/management, and monitoring of Alzheimer’s disease (AD)...

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3 min read

Risk Management in Pharmacovigilance

It’s important to know that whenever a new medicinal product is authorized based on specified indications at the time of authorization, the benefits...

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2 min read

Prioritizing Patient Safety and Fostering Innovation with the MHRAs New Roadmap for Medical Devices

On January 9, the United Kingdom (UK)’s Medicines and Healthcare Products Regulatory Agency (MHRA) released a regulatory framework – Roadmap towards...

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4 min read

Strategies for Successful Clinical Data Management Rescue Studies

What is a rescue study? A rescue study is a clinical trial that is being conducted by a new vendor after having previously been conducted by another...

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3 min read

The Role of Scientific/Medical Literature Screening and Review in Pharmacovigilance

Why search the scientific and medical literature?

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5 min read

Challenges for Medical Device Database Builds and Strategies to Overcome Them

What are some of the challenges with database builds for medical device studies, given the current regulatory requirements? What are the important...

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Automation and the Future of Clinical Data Management

Automation in clinical data management (CDM) is becoming increasingly popular due to the increasing volume and complexity of data being generated by...

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