Copyright © 2013 Darmantest Laboratories
Client
Participant
Participant
Client
Client
DarmanTest Laboratories and Research Center
Դարմանթեստ Լաբորատորիս Հետազոտական Կենտրոն

Darmantest Laboratories (DTL)
and
Quality Assurance
are Synonymous

 DTL strictly adheres to U.S. FDA, ICH and EMA 
 regulatory guidelines. 

 We recommend that potential clients that are 
 willing to sacrifice quality for price not contact
 us.
 
 We will offer very competitive prices, but we will
 not reduce the quality of our work  for a cheap
 price. 

 We are a young company and want your 
 business, but we will not lower our standards.

Study Design
Protocol
Method
Development
Method
Validation
M. of H. - IRB
Approval
Subject Select
Screening
Clinical
Phase
Pharmacokinetic
Statistical
Analysis
 Darmantest Laboratories (DTL) conducts Bio-Equivalence, 
 Bioavailability, or Pharmacokinetic Studies in full compliance with U.S.  Food and Drug Administration (FDA), European Medicines Agency (EMA), and International Conference on Harmonization (ICH) regulatory guidelines.
 
 From the initial inquiry to the final study report DTL works with you, as a partner, to achieve a high quality clinical study, in the shortest period of time and at a reasonable cost.




Final Study
Report
Our Services
     DTL Chemists