---
title: TGA PIC/S GMP Compliance Gap Analysis at Indian Pharmaceutical Company
description: SeerPharma to execute a 4-day inspection of pharmaceutical company manufacturing site against PIC/S GMP to help them achieve compliance for a TGA licence.
---

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# [TGA PIC/S GMP Compliance Gap Analysis at Indian Pharmaceutical Company](https://blog.seerpharma.com/pic/s-gmp-compliance-gap-analysis-for-indian-pharmaceutical-company-aiming-for-tga-gmp-clearance)

 Written by [SeerPharma](https://blog.seerpharma.com/author/seerpharma) | Jan 7, 2019 11:26:14 PM

**SeerPharma has been assisting an Indian Pharmaceutical company based in Gujarat with GMP facility design considerations. The company has now requested SeerPharma inspect their Operations against the PIC/S Guide to GMP, to help them achieve PIC/S GMP compliance. With GMP Clearance from the TGA and other regulators, the company will be able to export their product to Australia and other PIC/S Member countries. The mock inspection conducted by SeerPharma will look to identify any GMP compliance gaps that will need to be addressed prior to a regulatory inspection.**

****

SeerPharma will spend four (4) days on site inspecting the facility and operations, specifically targeting the following steps of manufacturing pharmaceutical product:

- Starting Materials - looking at activities such as how product is received and handled
- Warehousing – reviewing temperature control and areas used for storage
- Testing, Quality Control (Raw Materials and/or Finished Product)
- Processing or assembling – looking at activities such as dispensing and formulation
- Primary and Secondary Packaging
- Utilities and Services – reviewing services such as HVAC and Water Systems
- Release for Supply
- Validation activities for the Facility, Equipment and Computer Systems impacting product quality

SeerPharma has extensive experience identifying and addressing GMP compliance issues to help best prepare your team.

[Contact us](https://www.seerpharma.com/contact-us) if you are looking for support in your preparations to obtain a GMP License or GMP  
Clearance.

This post comes from our October 2018 Journal. [Click here to see more of our Journal content](https://www.seerpharma.com/about-us/journal), or click the links below to read other related posts:

- [CSV Gap Assessment for Pharmaceutical Distributor](https://blog.seerpharma.com/computer-system-validation-csv-gap-assessment-and-consulting-for-pharmaceutical-distributor)
- [TGA GMP License Assistance for a New GMP Facility](https://blog.seerpharma.com/tga-gmp-license-assistance-for-a-new-gmp-facility)
- [New GMP Facility Design, Qualification, Validation and TGA GMP License](https://blog.seerpharma.com/new-gmp-facility-design-qualification-validation-and-tga-gmp-license)
- [FDA and TGA GMP Inspection Help for Pharmaceutical Company](https://blog.seerpharma.com/fda-and-tga-gmp-inspection-help-for-pharmaceutical-company)
- [Assisting Indian Pharmaceutical Firms with Regulatory GMP Inspections](https://blog.seerpharma.com/assisting-indian-pharmaceutical-firms-with-regulatory-gmp-inspections)

[View full post](https://blog.seerpharma.com/pic/s-gmp-compliance-gap-analysis-for-indian-pharmaceutical-company-aiming-for-tga-gmp-clearance)

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