ISO 9001:2015   |   ISO 27001:2013

Project Management & Trial Planning

Central to the success of any project is an experienced project manager (PM) to lead the team. Clear communications between the sponsor and our MMS team members is also essential and our PMs along with our project leads are skilled communicators, ensuring clarity of scope, timelines, and responsibilities at the onset of every project. Throughout the planning and conduct of your project at MMS, you will see a results-oriented and proactive approach that will ensure project timelines are met and quality is maintained.

Each of our MMS team members acts with a Sense of Urgency and Leadership (SOUL), looking to ensure risks are identified early, appropriate preventative actions are taken, and when issues  arise, they are addressed quickly. We keep the big picture in mind and understand that each clinical trial, dataset, or report we deliver fits in the context of a larger development program and set of organizational goals.

The processes in place at MMS are continually refined. This includes looking across our joint process steps (MMS internal processes combined with our partner’s organizational processes) to identify ways we can streamline service delivery and reduce time for project completion. Our recommendations have resulted in significant enhancements, the removal of redundancies, and a reduced need for sponsor oversight activities. We strive to work as an extension of your organization.

The MMS quality management system adheres to strict ISO standards, requiring independent audits and certifications annually. Our project team members understand the value of these strong processes, peer reviews and quality checks and the resulting value this brings to our sponsors. The MMS business model is simple, and reflected in the aim of our colleagues and project teams – A successful delivery of each project, at the top level of quality and with the highest customer satisfaction.

Please see what our sponsor partners are saying about MMS…

Clinical Programming for the development of a clinical data warehouse –

“On behalf of the entire data warehouse team, I would like to thank you for your hard work, commitment over the last 2 years and for the expert support in finalizing these datasets. It was a pleasure to work with you and look forward to our next project together.”

– Team Lead, Large Global Pharma

Preparation of A Complex Pooled Clinical Study Report –

“Congratulations! I must say the pooled report has had a lot of challenges and this is incredible that we have finalized the report well in advance of the planned timelines. Once again, many thanks for your incredible efforts in getting this completed and leading our teams through the numerous reviews and discussions.”

– Manager, Regulatory Writing. Large Global Pharma

Statistical Programming for NDA submission –

“Thank you to your team for expediting the completion of the ISS data tables! Your contribution to the submission is truly invaluable”

– Sr. Manager, Biostatistics, Mid Sized Pharma

Preparation of Briefing Document for Type B Meeting –

“By the way, FANTASTIC JOB on this! I am extremely pleased that you carried this through to completion with a maximum of efficiency and a minimum of noise… the team was very pleased as well.”

– Manager, Medical & Regulatory Writing, Mid Sized Pharma

Regulatory Submission Support Based on Strong Science and Strength of Process. The difference is in the data!