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Trial Master File
At Tranquil Clinical Research, our team will ensure your essential documents are well completed and filed according to the requirements of the FDA and local regulations. We work with investigative sites to ensure compliance throughout the study period. Tranquil Clinical...
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Study Start-up
Launching a new drug or medical device can be a complex and expensive process. The majority of project efforts will go towards clinical development and research. Tranquil Clinical Research utilizes gap analysis to evaluate and prevent barriers to efficient deployment...
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Study Rescue
At Tranquil Clinical Research, we thrive where others struggle. We can rescue your study at any point throughout the clinical trial life cycle despite the challenges encountered. Feel free to contact us anytime; we will be more than happy to provide a...
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Regulatory Affairs
At Tranquil Clinical Research, our team is highly knowledgeable in global Regulatory laws and requirements that guide the conduct of clinical trials. We understand FDA requirements for clinical trials and work with global partners to ensure a shortened timeline from...
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Project Management
At Tranquil Clinical Research, we provide full Project Management support for all our clinical trials. A Clinical Project Manager (CPM) is assigned to each study as the primary point of contact with the Sponsor. Our CPMs engage with the client...
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Pre-Clinical Phase
The Pre-clinical stage can be one of the most pivotal stages in your research program and will have lasting impacts on your IND, NDA, Clinical Trials and beyond. We provide pre-clinical services and mentorship from highly knowledgeable and renowned Strategic...
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