Quality Document Templates
for GLP, GMP & GCP
For novel therapeutics to reach the clinic the investigator must satisfy the safety and efficacy requirements of the regulator. Much of the documentation used to meet these regulatory standards, particularly those that relate to facility or process compliance, is reproducible. Furthermore, this process of compliance is both time consuming and expensive with a full system often taking well over 12 months and $300,000 to create.
In an effort to reduce the cost and time burden of creating documents to meet this requirement TIA has established iQDOCs
, a world-first open access library of generic template documents for use in establishing and documenting research quality systems leading to accreditation.
The access model for iQDOCs is currently under consideration and registrations for access will soon open.