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Committed to
clinical development

DRC is specialized in assisting companies from market access strategy over clinical development strategy to the full setup and management of clinical trials. In parallel we offer clinical quality services ranging from audit services to the full development of quality management systems.

"For biotech, medical devices,
pharmaceutical industry and academic research."

Our mission

  • Our mission is adding value through a personalized approach ensuring success from the very beginning in clinical research.

  • As no two clinical develop-ment paths are ever the same, we at DRC, strongly believe in partnering with our client as of the transition from pre-clinical to clinical research.

  • This minimizes the risk of late-stage development failures, increases the probability that optimal safety and efficacy data are available and decreases the total time involved with drug or medical device development.

Our services

DRC is providing international services for drug and medical device development.

Clinical operations

Full management and conduct of clinical trials


  • Project Management
  • Monitoring Services
  • Regulatory
  • Patient recruitment
  • Data Management & Statistics
  • Medical Writing
  • Clinical Supply Chain
  • Pharmacovigilance
  • Lab services
Quality

QM consultancy, development and auditing services


  • Conducting sponsor and investigational site audits
  • Vendor assessments
  • Developing and optimizing Quality Management Systems
Consultancy

Transitioning from pre-clinical to clinical


  • TPP / Market Access Strategy
  • Clinical development strategy & Project Management
  • Regulatory strategy
  • Protocol/study design
  • Study Feasibility
Clinical operations

Full management and conduct of clinical trials

  • Project Management
  • Monitoring Services
  • Regulatory
  • Patient recruitment
  • Data Management & Statistics
  • Medical Writing
  • Clinical Supply Chain
  • Pharmacovigilance
  • Lab services
Quality

QM consultancy, development and auditing services

  • Conducting sponsor and investigational site audits
  • Vendor assessments
  • Developing and optimizing Quality Management Systems
Consultancy

Transitioning from pre-clinical to clinical

  • TPP / Market Access Strategy
  • Clinical development strategy & Project Management
  • Regulatory strategy
  • Protocol/study design
  • Study Feasibility
We provide solutions for your challenges.
Our Strenghts
  • Our personalized approach is key in our believe that we are not just a service provider but a trusted partner for the long-run.

  • Linking together consultancy, clinical operations and quality services within one partner significantly increases success rate and reduces time in conducting clinical research by providing fully integrated solutions in clinical product development.

  • Our high-quality standards and continuous investment in tools and expertise, ensures delivery within the expected timelines and an all-time inspection readiness. We bring Sponsor, CRO and sites together in a regulated and validated cloud environment.

  • We have immediate access to an extensive international network across the healthcare industry.

  • Our senior management and key staff are all directly involved in customers projects and draw on experiences ranging from 10 to 25 years of working in the life science industry.

  • We add value through optimizing the transition from pre-clinical to clinical.