DZS provides a wide range of services for the pharma, biotech and medical device industries.

Clinical Development Strategy

Expert consultation, strategic direction and responsive communication to help guide your clinical trial.

Clinical Operations

Clinical Project Management

Utilizing proven clinical project management principles to effectively achieve milestones, meet timelines and optimize resources.

Clinical Monitoring

Identifying optimal sites and investigators for trials and providing ongoing support to ensure success.

Data Analytics

Clinical Data Management

Data management services emphasizing compliance to industry standards including GCP/GCDMP, 21 CFR Part 11, as well as ISO and CDISC standards, as applicable.

Medical Coding

Integrating with MedDRA, WHO DD Enhanced, COSTART, WHOART, ICD9 and ICD10 as well as customized dictionaries.

Medical Writing

Communicating the results of clinical development programs with expertise, flexibility and timeliness.

Biostatistics Support and Statistical Programming

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.

Medical Affairs

Supported by an experienced team, our medical affairs department is prepared to assist your post-marketing activities and market access challenges.

Medical Call Center + Pharmacovigilance

Medical Call Center

DZS Clinical Services is proud to offer its 24/7, US-based medical call center that is ready to handle your pharmacovigilance needs. Global support is offered by our offices in Finland, India, Japan, and South Africa should international needs arise. Our organization can provide the QPPV role in the EU as required.

Pharmacovigilance

Our team of clinical research professionals bring decades of experience working with regulatory authorities worldwide including the FDA and EMA. With DZS Clinical Services as your partner in pharmacovigilance, you can rest assured that all levels of safety data will be handled with the utmost care and attention to detail.

Strategic Outsourcing Solutions

Full-service Outsourcing

Providing full-service outsourcing models for all functions of your program, including trial conduct, data collection and analysis, oversight and reporting.

Custom FSP Models

Driving clinical development forward by managing specific clinical functions and teams to control costs and add flexibility.

Clinical Sourcing and Staffing

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.