An audit is a systematic and independent examination and disciplined approach to evaluate and improve the effectiveness of a system. Audits are carried out in order to verify that the individual elements within the system are effective and suitable in achieving the stated objectives.

We have almost experience of about 70 Audit experience with our expertise team. Since our expertise team has developed complete set of SOPs, Agenda, formats and check list to facilitate any type of Audits

c-GMP

Authorizer/Applicant and Importer are responsible to ensure that the respective manufacturing sites comply with cGMP. Our qualified auditors are available to take care of your responsibilities.

  • Vendor Audit
  • Deficiency Audit
  • Pre-regulatory compliance Audit/Mock Audit
  • For Cause Audits

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BA/BE Studies Monitored

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GCP Audits Conducted

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GMP Audits Conducted

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Training & Consulting Programs
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