Clinical Operations - QPS Custom-Built Research Services

Clinical Operations Overview

QPS Clinical Operations supports drug development in every clinical stage with a strong focus on Phase II-IV clinical trials and medical device studies.

QPS Clinical Operations offices are located in the USA. Austria, Croatia, Czech Republic, Germany, India, Netherlands, Spain, and Taiwan.

We conduct and manage clinical studies in accordance with International Conference on Harmonization-Good Clinical Practice (ICH-GCP) standards and all applicable regulatory requirements to pharmaceutical and scientific clients.

QPS_Clinical Trial Experience_Global_2023 v1

Clinical Trial Experience
Global 2023

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Clinical Research Services
Global 2023

CLINICAL TRIALS KIT

QPS has added a new capability, building clinical trial kits. We offer individualized service, fast turnaround times, and can ship to any global clinical trial site. Contact Us (link to contact form) for more information.

DATA MANAGEMENT

Data management for successful clinical trials. Data management is a fundamental element of a successful trial. This step is critical to your success.

MEDICAL WRITING

High-quality medical writing is important to the regulatory success of our clients. Our medical writing writers have the therapeutic expertise necessary to deliver high-quality written material.

PHARMACOVIGILANCE

At QPS, we have systems in place to enable the identification, recording, reporting and analysis of safety information so that any safety signals that arise during a trial are quickly identified and acted upon.

PROJECT MANAGEMENT

Proven success in clinical trial project management. QPS will meticulously manage your late phase II-IV clinical research from start to finish.

SITE MONITORING AND MANAGEMENT

Effective clinical trial site monitoring and management. Proper site management is an essential element of clinical trial execution and in ensuring trial success.

“We have had overall wonderful experiences with the QPS team, which is why we continue to establish new projects with you.”

– QPS Client

“We are extremely grateful and pleased with all the work over the last month from Anant Pedada, Lan Li, Sarah Patterson, Dave Quirico, and all the QPS QA folks. We could not have completed any of these studies without their help and willingness to meet our tight timelines. All of our efforts right now are on our submission. If we get approved, we should have some more studies to send you.”

– QPS Client, Study Director

“Thank you so much for all of your support on this program! We really appreciate the time and effort you have put in. The effort has been such a collaborative journey, and your expertise has been invaluable. We look forward to continuing our collaboration on our other studies with you.”

– QPS Client

“I wanted to say thank you to the QPS team for all of your hard work and efforts to complete the study analysis during what has been a very challenging year to date. You delivered the reports to the new agreed timeline and these were of a high quality.”

– QPS Client

“Thank you for making all the changes within our requested timeline. The updated dataset looks great! We greatly appreciate your efforts in helping us to meet our study timelines.”

– Joshua H

“Molly and I both really appreciate the extra time and effort the QPS team made in getting this document turned around so quickly. Job well done!”

– Lisa L

“Thank you very much for delivering the QC’ed data by timeline. It is great to work with you and your team.”

– Lei L

“Thank you again for the very nice draft report.”

– Karen V

“This application required exquisite organization, teamwork and perseverance. We submitted about 350 pages of highly scrutinized regulatory documentation. Especially considering that we received only a couple minor requests for updates, this was an impressive effort.

Such a high-quality submission, followed by a similarly high-quality pre-clinical, non-clinical and CMC program, along with high-quality QC, organization, summaries and interpretation of dozens of reports; all accomplished just about a year after we nominated the clinical candidate.

Thank you for your contribution to the successful delivery of this historic company milestone.”

– President and CEO

“Thank you for the fast turnaround! This file concludes all data transfers for study … are complete. Thank you for another successful collaboration!

– Jennifer M

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