Clinical Research Services - Credentials


Regulatory Approvals

Reliance Life Sciences' facility, systems and processes have successfully completed several regulatory inspections. The facility and studies have been inspected and audited by the following agencies:

  • DCG (India) - BA/BE facility
  • FDA (US) - BA/BE studies
  • ANVISA (Brazil) - BA/BE facility
  • Austrian Agency for Health and Food Safety (Europe) – BE studies
  • MPA (Sweden) – BA/BE studies
  • MOH (Turkey) - BA/BE facility
  • MOH (Israel) – BA/BE studies
  • MOH (Belarus) – BA/BE studies
  • NPRA (Malaysia) – BA/BE studies
  • OECD & GLP - Toxicology Center
  • NABL - Molecular Diagnostics Laboratory
  • CAP - Central Laboratory
  • CLIA - Central Laboratory

Quality Assurance (QA)

Reliance Life Sciences has an independent Quality Assurance Group.

The QA group is involved in handling various QA activities including SOP management, training management, vendor management, conducting and reporting audits, computerized system validation, change control management, deviation management, CAPA management, hosting external audits/inspections and handling queries for several regulatory agencies. Audits performed by QA auditors include project specific audits (clinical, bioanalytical, statistical and reporting phase), system/process audits and vendor (qualification/re-qualification) audits. Audits are conducted to ensure systems/processes are in compliance and study data generated is in compliance to GxP standards, applicable regulations, in-house SOPs and study protocols.