Extensive expertise
MEDIS offers tailored solutions for biotech, pharmaceuticals, and clinical development needs.
MEDIS is a leading medical advisory company that offers a comprehensive range of services to support businesses in the healthcare industry.
Our team of experts is committed to providing the highest quality Clinical Development, Medial Affairs, PV/Drug Saftey, Data Managment, Medical Writing, EDC System, Information Technology to help businesses achieve their goals and objectives.
At MEDIS, we understand that businesses need to stay ahead of the curve to succeed.
What we offer
Clinical Development
an outsourcing model that offers pharmaceutical, biotechnology, and CROs to access to specialized expertise and resources for conducting clinical trials. CDaaS providers manage the end-to-end process of clinical development, enabling faster, more cost-effective product development and regulatory approval.
Medical Affairs
Medical Affairs is a key function within pharmaceutical, biotechnology, and medical device companies that bridges the gap between clinical development, healthcare providers, and the market. It plays a crucial role in ensuring the safe and effective use of a product through medical and scientific engagement.
Data Management
Data Management in clinical development refers to the systematic collection, processing, and storage of data generated during clinical trials. The goal is to ensure the accuracy, integrity, and security of the data throughout the trial process, which is critical for regulatory submissions and decision-making regarding the safety and efficacy of a drug or medical device.
Drug Safety
also known as pharmacovigilance, is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. Ensuring drug safety is crucial for protecting patient health and ensuring that medications are used safely and effectively.
We offer comprehensive medical writing services, including protocol development, clinical study reports, patient informed consent forms, manuscripts, and all protocol related documents for regulatory submissions.
Medical Writing
EDC System
An Electronic Data Capture (EDC) System is a software solution used in clinical trials to collect, manage, and store data electronically, replacing traditional paper-based methods. EDC systems streamline data collection processes, enhance data accuracy, and improve overall efficiency in clinical trials.
Information Technology
Information Technology (IT) in Medicine refers to the use of technology to improve healthcare delivery, streamline medical processes, and enhance patient outcomes. IT solutions in medicine cover a wide range of applications, from electronic health records (EHRs) to telemedicine, and play a vital role in modernizing healthcare systems.
About Medis LLC Services
At Medis LLC, we support biotech and pharmaceutical advancements through tailored services in clinical development, medical affairs, drug safety, and data management.
Our Expertise
We provide specialized support in EDC systems, medical writing, and information technology to empower life sciences and enhance development outcomes.