Our Blog | Halloran

Risk-based monitoring in clinical trials: Implications for sponsors, investigators

Monitoring risk is certainly not a new concept in healthcare. There are countless treatment protocols and care pathways designed to mitigate risks for patients and making their treatment safer. More recently, many of these risk management discussions are focused on clinical trials.

Revamping the vendor qualification process for clinical stage outsourcing

Consumer awareness of the quality of goods purchased is good practice in any industry, but in biotech and pharma, it is a regulatory requirement. One of the most common goods we purchase in this industry is a vendor’s services — their time, effort, and resources.

Cloud-based COTS Solutions are Pharma’s Future in Research

Business, technical, and financial incentives are driving the rapid adoption of cloud-based, commercially available solutions in pharmaceutical research and operations. With it, broader cloud-based solutions and integration platforms are emerging.

The life of a virtual clinical trial participant

I am currently participating in a clinical trial. I have neither seen a physician nor traveled to a site for a procedure. During my first 15 days of trial participation, my samples have been sent 43 times - and I never once had to leave my house for it.

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