MMS is a unique CRO with group of scientific writers who are subject matter experts in nonclinical area and regulatory writing. Understanding of the regulatory laws and guidance as it applies to nonclinical program development and nonclinical regulatory submission documents is crucial given the growing complexity of drug development and changing regulatory requirements. Multiple nonclinical studies are required to determine the safe dose for a first-in-human (FIH) study and collect safety data in the development of any new disease treatment. Nonclinical evaluation is a key component of drug development. MMS’ medical writing technology currently includes SmartStart ™ tech-enabled templates and Automatiqc ™. Our proprietary technology is used by MMS experts to increase writing efficiency and quality of in-text tables in the documents, build productivity of quality control, and lower the risk of errors in the documents.
#Mms holdings medical writer salary software
The MMS team focuses on continuous improvements through technology-aided authoring software to streamline the medical writing process, including the use of immutable tables in the documents. “from day one, we were impressed with the efficient and smart decisions brought forth by MMS to bring this drug to market.”
Our team’s professionalism and expertise are reflected in the positive feedback from Sponsors, e.g.
The success of MMS Medical Writing teams is built on strong processes, uncompromising quality standards, and a dedication to ongoing education at all levels. Our expertise spans across various therapeutic areas and all phases of drug development including nonclinical (preclinical), CMC, clinical, regulatory, safety, and medical communications documents. Our writing team supports Sponsors on project level or across writing pipelines including Functional Service Provider (FSP) relationships.
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MMS offers the largest number of writers with a full range of experience and in-depth knowledge of laws and regulations across regions in the industry.
MMS has a strong global presence in regulatory and medical writing services to consistently produce cohesive, quality focused, and scientifically accurate documents.
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