Welcome to Medkine
Medkine was established in 1990 with the straightforward aim of offering precise, dependable, and prompt solutions to meet the data requirements of clinical trial professionals. Currently, we operate as a comprehensive technology-driven Contract Research Organization (CRO) with a demonstrated history of providing client-centric services, along with cutting-edge solutions utilizing technologies such as Machine Learning and Analytics, tailored for Pharmaceutical, Biotechnology, and Medical Device companies.
We support companies in the Pharmaceutical, Biotech, and Medical Device sectors through our distinct "people + product" service model
For over three decades, the Clinical Data Management division at Medkincro has been providing reliable and cohesive data management solutions to companies.g the commonly utilized EDC systems.
Medkincro has successfully delivered SAS programming and proficient statistical analysis throughout all phases of drug development across various therapeutic areas.
Keeping our clients' goals at the forefront, Medkincro delivers flexible, efficient, and customized SAS programming solutions. Our offerings can cater to both comprehensive studies and tailored services.
Medkincro is a trustworthy global partner for pharmacovigilance and drug safety services, offering biopharmaceutical companies safety solutions for pharmaceuticals, medical devices, vaccines, and cosmetics.
Organizations can leverage CDISC, SDTM, and ADaM standards for their internal processes and regulatory filings by utilizing Medkincro's pool of Clinical Data Standardization subject matter experts.
REASON FOR CHOOSING MEDKINE CDM
The CDM Unit at Medkine places great importance on high-quality data. Nonetheless, we recognize the value of your time and budget. With the assistance of our committed team leaders, you can handle data that aligns with our rigorous standards. We pride ourselves on our consistent accuracy, constant availability, and commitment to cost-effectiveness. Our specialized offerings are designed to enhance the quality, consistency, and integrity of your clinical trial data.
Medkincro has a track record of success working with major biotech and pharmaceutical businesses spanning xx years. Our customers can speak to the fact that we believe in scalability and cost-effectiveness through automation and work to automate as much as feasible in the clinical development life cycle..
Medkincro has a track record of success working with major biotech and pharmaceutical businesses spanning xx years. Our customers can speak to the fact that we believe in scalability and cost-effectiveness through automation and work to automate as much as feasible in the clinical development life cycle.
Medkincro has a track record of success working with major biotech and pharmaceutical businesses spanning xx years. Our customers can speak to the fact that we believe in scalability and cost-effectiveness through automation and work to automate as much as feasible in the clinical development life cycle.
Medkincro has a track record of success working with major biotech and pharmaceutical businesses spanning xx years. Our customers can speak to the fact that we believe in scalability and cost-effectiveness through automation and work to automate as much as feasible in the clinical development life cycle.
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