Safety pharmacology | Nonclinical Study Design | First-in-Human | Pharmacology and Toxicology | SOP Development – Consultancy:

Drik has, experienced team and whose global reach includes a network of sponsors from the U.S., Europe, India and China. We assist small and large pharmaceutical, cosmetics, chemical, and tobacco industry by providing timely approach that helps further in their development. We deliver quality of services to meet their regulatory requirements.

We provide service in

  • Nonclinical study design, implementation and monitoring 3rd party CROs (First-in-Human trials, proof of concept)
  • Short term and long term toxicity studies
  • Review data, data interpretation (study reports, literature)
  • Database mining, Software tools, SOP development
  • Pharmacology and Toxicology
  • Guidelines on GLP studies, Clinical research, Regulatory affairs
  • Preparation/review of preclinical sections of regulatory documents
  • Education and training

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