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CRD TEAM

Suppository

  • Experience of conducting multiple studies with suppositories.
  • Database of compliant volunteers with experience of previous participation in same type of studies.
  • Trained and experienced staff with procedures to conduct dosing procedures.
  • Clinics and pharmacy with controlled temperature and humidity to facilitate IMP handling.

Our exemplary regulatory track record

USFDA
33 times
Brazil ANVISA
7 times
WHO
5 times
UK MHRA
3 times
EU - AGES
1 times
South Africa - MCC
1 times
NPRA - Malaysia
4 times
DCGI
13 times