About Us

Who We Are?

Completum Clinical partners and collaborates with innovator Research & Development companies to co-develop therapeutic and preventative drug, biologic and medical device products in the clinical phase of the development process.

Jack Minster joined DSG, Inc., the clinical data software and services company in 1999, as the Vice President of Sales and Marketing to lead DSG’s growing business development operations. To resolve challenges faced by his clients, Jack was instrumental in developing the industry’s first RTSM system organically integrated with EDC; also the world’s first electronic source system which lead to the FDA’s first-ever eSource-approved drug in 2008; and the first CTMS offering online monitoring trip reports. DSG ...

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What We Offer!

Medical & Safety

Completum Clinical partners and collaborates with innovator Research & Development companies to co-develop therapeutic and preventative drug, biologic and medical device products in the clinical phase of the development process.

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Investigative Sites

Global network of dedicated and strategically located high enrolling Phase 1 - 3 international clinical trial investigative sites, operating under the maxim Experience-Integrity-Quality ...

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Why Choose Us?


  • Vice President Medical and Scientific Affairs
    Their excellent handling of Medical Monitoring and Drug Safety throughout the course of the clinical development program gave us excellent clean data that greatly helped our company on the approval pathway of our drug product  
    Vice President Medical and Scientific Affairs
    Biotech company
  • Senior VP Regulatory Affairs
    Their understanding of the drug safety regulatory environment based on their 20+ years of direct working experience with the US FDA turned out to be a great asset for our clinical trials  
    Senior VP Regulatory Affairs
    International CRO
  • Pharma Company
    Proactively managed the safety monitoring of our company's clinical development program that helped us achieve our corporate objectives much earlier than our projected timelines" VP of Clinical Development mid-sized
    Pharma Company
  • Pharma Company
    I completed my review of your report, and I am lost for words. Thank you so much for capturing such thorough details. This is the most comprehensive report I have ever reviewed. I have no follow-up comments so I will move forward with approving.
    Pharma Company
  • Pharma Company
    Our monitor is a pleasure to work with and has been very flexible with her schedule to accommodate our needs. Her trip reports have been completed in a professional and timely manner. Her communication style is very effective, and she easily developed good working relationships with the sites she was assigned to. I am currently reviewing our resourcing needs and will reach out to her with new opportunities.
    Pharma Company
  • Medical Device Company
    Our monitor has been very flexible with his schedule to accommodate our needs and has been a great asset to the study team. He is very detailed and offers great insight. It was a pleasure to work with him.
    Medical Device Company
  • European CRO
    Working with the monitor has been and still is an absolute pleasure. The assignment was with one of our toughest, non-responsive sites to work with, but she has remained professional and respectful in the most challenging of times.
    European CRO
  • Clinical Project Lead
    Thank you for all your support. This was my first time working with a printer. It was great to have someone so knowledgeable in clinical research work to help guide me through the process. I will contact you for help with another study I will be working on soon.
    Clinical Project Lead
  • European CRO
    Our contract monitor has been doing some Lead CRA work for us (which I am hugely grateful for)… I want to thank you for bringing her to us. She is an exceptional resource.
    European CRO
  • Clinical Project Director
    I just wanted to contact you about the stellar support Kathy and the CIP production team provided for our order. They made it possible to meet very tight SIV timelines for this study. Kathy found several file issues and alerted us. We provided updated files in the 11th hour; she made the changes and sent new proofs in time to produce and ship the materials in time to arrive the day before our SIV. This request went from Rush to Super Rush and your team kept its commitment. It is so great working with a vendor that understands our work and is as committed as we are. Thank you!
    Clinical Project Director
  • Director of Clinical Affairs
    He feedback from all of us is that you have given us some great monitor candidates to interview, and we really appreciate it.
    Director of Clinical Affairs
    Medical Device Company
  • Stan Bukofzer
    I just wanted to reach out and share how impressed I and the team have been with Yan. It’s been an absolute pleasure working with her. She has been superbly responsive and very helpful in clarifying requests, sometimes suggesting alternate cuts that might be more helpful. In summary she is great to have on the team. Many thanks
    Stan Bukofzer
    Chief Medical and Scientific Officer
    Ocelot Bio
  • Mike Nelson
    Your team exceeded all expectations throughout our Phase 1 and Phase 3 projects. Responsiveness and proactive suggestions were off-the-charts. No matter where my career may take me, I promise to take you and your team with me.
    Mike Nelson
    Sr. Director, Clinical Operations at Alexza Pharmaceuticals

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