We are proud to share that the regulatory team at MMS has been selected as one of three top finalists in the Fierce CRO Awards for Leadership in Regulatory Compliance! The Leadership in Regulatory Compliance category recognizes CROs that demonstrate exemplary adherence to regulatory standards and guidelines, ensuring compliance and facilitating smooth regulatory submissions. With zero refusals to file since inception, MMS has been instrumental in helping Sponsors successfully bring more than 50 submissions to global health authorities in the last five years, including INDs, NDAs, and BLAs. Read the full press release for details: https://lnkd.in/gYRbRAns #OneMMS #PharmaceuticalIndustry #ClinicalResearch #DrugDevelopment #RegulatoryStrategy #NewDrugApproval CC: Fierce Pharma, Fierce Biotech
关于我们
MMS Holdings (MMS) is an award-winning, data-focused clinical research organization (CRO) that supports the pharmaceutical and biotech industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, an 18-year track record, AI technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner. With a global footprint across four continents, MMS maintains an industry-leading customer satisfaction rating. For more information, visit www.mmsholdings.com
- 网站
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https://www.mmsholdings.com
MMS的外部链接
- 所属行业
- 制药业
- 规模
- 501-1,000 人
- 总部
- Canton,MI
- 类型
- 私人持股
- 创立
- 2006
- 领域
- Clinical Strategy & Execution、Regulatory Affairs and Submissions、Clinical Programming & Biostatistics、Data Management、Clinical Trial Disclosures、Medical Writing、GCP Auditing、clinical research organization、Use of Real World Evidence、Pharmacovigilance & Drug Safety、Quality Control、Quality Assurance和Data Science
地点
MMS员工
动态
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What does it take to design effective clinical trial protocols? We have an answer for you. From minimizing risks to simplifying operations, well-crafted protocols are the foundation of successful clinical trials. Thoughtful design does 3 things well. It: ? ensures regulatory compliance, ? improves patient outcomes, and ? boosts operational efficiency—setting trials up for success from the start. Explore strategies for better trial design and protocol development in our Perspectives blog article: https://hubs.li/Q02Z0lpv0 #ClinicalTrials #ProtocolDevelopment #ClinicalResearch
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Meet Sasha Chetal! A remote Project Manager at MMS, hailing from Aberdeen, Scotland. Renowned for her exceptional white glove service, Sasha brings a decade of industry expertise to her role. She skillfully directs and manages the scientific, technical, and operational facets of projects in diverse therapeutic areas, including neuroscience, oncology, infection, respiratory, rare diseases, and inflammation. Sasha holds a Master's in Veterinary Microbiology, leveraging her extensive experience in translational research to consistently "Wow the Customer" - an embodiment of one of our core values at MMS. Discover more about our solutions and feel free to ask for Sasha by name: https://hubs.li/Q02Yvm980 #OneMMS #neuroscience #oncology #rarediseases
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We are thrilled to announce that MMS has once again been recognized as a Top Workplaces award winner by the Detroit Free Press and the USA TODAY Network! This honor is especially meaningful because it reflects the voice of our employees. Over the past year, the Top Workplaces survey gathered insights from more than 2 million employees across 8,000+ organizations—and MMS continues to stand out as a place where innovation thrives, collaboration excels, and people are truly valued. To our incredible team: Thank you for bringing your dedication, expertise, and passion to work every day. Celebrate with us in the comments!?For full details on the win, read here: https://lnkd.in/gnzhsC5Z #TopWorkplaces #OneMMS #DrugDevelopment
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Strong partnerships start with expertise and teamwork! From day one, MMS has focused on delivering the right support to drive meaningful progress, ensuring every step leads to impactful outcomes. Explore our Biometrics solutions, for instance, where the advantages that MMS brings include better trial data execution, lower risk, stronger submissions, and accelerated outcomes. Let's explore how we can advance your next Biometrics project: https://hubs.li/Q02Yvrk-0 #SponsorsSay #ClinicalResearch #ClinicalData
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ICYMI: MMS was recognized with EcoVadis Bronze Medal for leadership in ESG sustainability efforts as a leading CRO! Ben Dudley, MMS Chief Commercial Officer, shared, “MMS is one of the few CROs that has been ISO certified since inception, and our dedication to deep processes, sustainability, and ethical practices remains integral to our approach. From reducing environmental impact in trial designs to fostering a diverse, inclusive, and ethical workforce, we are working to set new standards for what it means to be a responsible CRO partner.” Read more about this award and our commitment to sustainability: https://hubs.li/Q02Ykvb80 #Sustainability #ESG #Leadership #Pharma
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Do you need help in turning around distressed studies and getting them back on track? With MMS Transition & Rescue Solutions, our biometrics and regulatory experts take the burden off your shoulders and ensure a smooth, pain-free transition—without significant delays or budgetary concerns. Our keys for a successful rescue include: ?? Transition process management, and a well-established playbook to mitigate any risks for you and ensure smooth continuity. ?? Seamless technology transitions, ensuring that technical challenges are resolved quickly through in-house resource and leading-edge innovations for minimal disruption. ?? Regulatory gap analysis that goes beyond just fixing immediate issues to gain a proactive assessment of your data for regulatory compliance. When quality, compliance, and timelines are at risk, MMS is here to help. Read our latest thoughts on rescue work here: https://hubs.li/Q02YcGYc0 #ClinicalTrials #CRO #ClinicalResearch #DataManagement #Pharma #DrugDevelopment #ClinicalData #OneMMS
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Building strong, reliable partnerships is no small feat in clinical research! We like to prioritize responsiveness and high-quality service, working collaboratively with you to ensure that every project is delivered efficiently and with precision. Looking for a partner you can count on? Review our solutions: https://hubs.li/Q02Y2w980 #SponsorsSay #ClinicalOperations #Pharma
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Hear from Chrissy Manley in our latest perspectives article on a REMS Logic Model! Last week, the Small Business and Industry Assistance (SBIA) program in the Center for Drug Evaluation and Research (CDER) hosted a highly informative webinar on this model in REMS Design, Implementation, and Evaluation. Our recap of the webinar provides a view on the benefit of logic models, as documented in the FDA's draft guidance document published in May 2024. Read the full article here: https://lnkd.in/gZUM2XqC #REMS #FDA #CDER #DrugDevelopment
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This Veteran's Day, MMS would like to extend heartfelt gratitude to veterans in our communities in the US and across the globe. We recognize the sacrifices made by those who have served, as well as the invaluable contributions they continue to make in every aspect of life, including within our own ranks. The #OneMMS team is deeply committed to advancing meaningful work that supports our veterans. This year, we proudly contributed to a groundbreaking NDA submission for PTSD therapy with MDMA, a promising treatment for PTSD—a condition that affects veterans and countless others. To reference this work, click here: https://hubs.li/Q02XsYb20 To our MMS veterans and the global community of service members: thank you for your service, courage, and resilience! We honor your dedication today and every day. ?? #VeteransDay #Gratitude #PTSDResearch