PharmaInspect US is Globally professional pharmaceutical consultancy firm responsible for conducting the third party audits i.e. Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), Good Clinical Practice (GCP), Good Distribution Practice (GDP) and Good Pharmacovigilance Practice (GVP). The company is having experience of over 8 plus years in Pharmaceutical consulting across the geographies such as the UK, Europe, Asia, Brazil & USA. PharmaInspect US has proven its outstanding expertise and services to the clients in more than 25 countries.

Step 1
After conducting the audit we will share the audit summary report to the client. The timeline will be 1 week.
Step 2
Detailed audit report prepared by auditor. This will be provided within 30 days from the audit date.
Step 3
CAPA follow-up and review will be performed by auditor or audit coordinator. This will be performed by 1 week of time.
Step 4
All our audit summary reports and detailed reports are reviewed by our technical team.
PharmaInspect US has a Team of Very Experienced and Highly Qualified Consultants and Auditors Who are Certified From Internationally Recognized Bodies for providing Different Types of Services/ Audits. Such internationally recognized bodies are IRCA-CQI, ASQ, APIC, BSI etc. Currently, over 25 highly Qualified consultants/ auditors are associated with us who are based mainly in UK, EU, India, China, Brazil, USA etc.


