DZS provides a wide range of services for the pharma, biotech and medical device industries.
Expert consultation, strategic direction and responsive communication to help guide your clinical trial.
Data management services emphasizing compliance to industry standards including GCP/GCDMP, 21 CFR Part 11, as well as ISO and CDISC standards, as applicable.
Integrating with MedDRA, WHO DD Enhanced, COSTART, WHOART, ICD9 and ICD10 as well as customized dictionaries.
Communicating the results of clinical development programs with expertise, flexibility and timeliness.
Adding value to clinical protocols, market research projects and health economic outcomes research programs. Using an SAS® platform, DZS has the tools and expertise to produce quality deliverables including CDISC for all phases of drug and device development.
Supported by an experienced team, our medical affairs department is prepared to assist your post-marketing activities and market access challenges.
Providing full-service outsourcing models for all functions of your program, including trial conduct, data collection and analysis, oversight and reporting.
Driving clinical development forward by managing specific clinical functions and teams to control costs and add flexibility.
Leveraging a global network of clinical research professionals with vast industry expertise to provide broad recruiting services across a range of clinical development positions and geographic locations.