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| Veeda Oncology’s independent global Quality
Assurance department is staffed by a team of
experienced QA professionals in North America,
Europe and India. The QA department is entirely
separate from and independent of the personnel
engaged in the direction and conduct of clinical
trials. |
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| We perform audits in all stages of the
project: |
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- Protocol audit
- Trial master file (TMF) audit
- Investigator site audit
- Database audit
- Report audit
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| Internal systems audits include a
comprehensive review of procedures and processes
followed in the management of clinical trials
and are geared towards the identification of
weaknesses, as well as increased efficiencies. |
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| All audits are performed to assess adherence
and compliance with Standard Operating
Procedures (SOPs), Good Clinical Practice (GCP)
guidelines, regulatory requirements, the trial
protocol, client instructions, and contractual
obligations. |
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