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Jeremiah Rehm

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Jeremiah Rehm
Jeremiah Rehm
Clinical Solutions Specialist

Jeremiah has been an innovator in Life Sciences for more than 13 years -- the last 8 of those designing and maintaining Clinical Trial Management Systems. Prior to joining Bioclinica, he was a technology consultant and led the product management team for eClinical products acquired by Bioclinica. One of Jeremiah's specialties is in the use of Microsoft applications to consolidate and analyze operational study information, including translation of this data into meaningful performance metrics.

Blogs

Regulatory authorities require clinical trial progress to be monitored. The site visit report, known as the Monitor Visit Report (MVR), is where sponsors provide evidence that all regulated activities have been completed along with documentation of the outcome. These reports are open to regulatory inspection at any time during a study, as well as after, and even post product approval.

CTMS and MVR, Across the Great Divide
As anyone in pharma knows, our industry is undergoing major change; clinical trials are rapidly evolving and eClinical technologies are becoming more sophisticated by the day. Meanwhile site monitoring continues to be one of the most critical, costly, and labor-intensive activities in a clinical trial. Looking for a better way to address this, many organizations have made the switch from conventional CTMS to the "Microsoft Office-Smart" model.

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Leader in Clinical Trial
Management Solutions

Successful clinical trials require the ability to see key details and uncover hidden insights. Bioclinica utilizes science and technology to bring clarity to clinical trials, helping companies to develop new life-improving therapies more efficiently and safely.

Bioclinica SMART Our Digital Customer Portal Allows Sites and Sponsors to Benefit from Real-Time Access to Their Tr… https://t.co/VJi2kVttFu
Bioclinica (13 hours ago)
Bioclinica will be gold sponsors at the upcoming World Drug Safety Congress in Europe. Meeting with our team to le… https://t.co/7efqU3ZHb8
Bioclinica (2 days ago)
Bioclinica Cardiac Safety Services Offered a Unique Solution for a Specific Regulatory Requirement. Read our case s… https://t.co/4j1AUk6YDz
Bioclinica (5 days ago)
Agile IRT is here! How can you benefit? Download our webinar to know more. #bioclinica #irt #clinicaltrials… https://t.co/zH5aFYxxUf
Bioclinica (6 days ago)
Bioclinica's Electronic Data Capture #EDC has been used in thousands of clinical studies worldwide. Why? Our single… https://t.co/g427VOUSFS
Bioclinica (1 week ago)
Bioclinica will be exhibiting at the upcoming #SCDM2019 – the industry’s largest clinical data management event of… https://t.co/JLTSWOI8rl
Bioclinica (2 weeks ago)