Preferred partner for Pharma GxP audits 

Consistent, timebound, reliable partner for performing Pharma GMP audits and supplier qualification on behalf of client

ABOUT
Avasar Pharma is a fast growing enterprise based out of Bangalore. It is run by Pharma Quality professional having three decades of wide experience in Quality, supplier audits and regulatory inspections like USFDA, TGA, PMDA, Health Canada and ISO 9001:2015.

Our main focus is supporting our clients in performing GMP audits covering APIs, key starting materials (KSM), medical devices and drug products.

In addition to GMP audits, AVASAR supports in sourcing of APIs, pharma intermediates and nutraceuticals from regulatory approved manufacturers.


Services
- GxP Audits
- Sourcing of APIs and Intermediates

Our mission is to carry out thorough audit to assess GMP compliance in the Pharmaceutical Industry. AVASAR works closely with clients, providing a personalized approach tailored to their specific needs.
GxP Audits
(A) Support our clients in performing Third Party Audits by Subject Matter Experts having experience in audits. Since inception in 2022, good number of supplier audits were done for overseas clients, EU and US clients.
Services are not limited to audits, AVASAR supports in sourcing also.
Sourcing of APIs and Intermediates
(B) Quality, Regulatory and Compliance requirements are constantly increasing. We support our customers and business partners in meeting these challenges and help in sourcing of APIs and Pharma Intermediates from GMP and regulatory approved manufacturers.  

Why choose our services

Why choose our services

AVASAR offers top-notch, customer-focussed solutions that set us apart in quality, cost-effectiveness and reliability. Your trust is important to us.

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Third Party Audit, Vendor Qualification

As per regulatory requirements Pharmaceutical companies need to assess, qualify and perform GMP audits of their suppliers periodically. We are here to support in performing audits through experienced auditors. Once the audit is contracted by the client, we finalize the audit day/s with manufacturer considering client's deadlines and requirements.

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Audits performed-Year 2024-2025

GMP audits

Audit standards for Supplier Qualification, Facility Approval for Drug Product Transfer

Audit Standard applied

Audits performed in India for clients across the globe

Updated- Jun 25

Active Drug Substance (API), Pharma Intermediates and Nutraceuticals

Active Drug Substance (API), Pharma Intermediates and Nutraceuticals

Associated with manufacturers having regulatory approvals from WHO GMP, USFDA, PMDA, TGA, COFEPRIS, ANVISA and FSSAI. As we are under discussions for more products from regulatory approved manufacturers, feel free to contact us for products that are not there in our present product list.

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APIs- List 1

The Active Drug Substances (APIs) service ensures that our clients have access to a reliable and consistent supply of essential pharmaceutical ingredients.

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Pharma Intermediates - List 1

With our Pharma Intermediates service, you can count on reliable sourcing, consistent quality, and timely delivery to support your pharmaceutical manufacturing operations.

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Pharma Intermediates - List 2

From regulatory approved manufacturing site

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APIs - List 2

From international regulatory approved manufacturing sites

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Murthy Avasarala

Founder - Director - Business Development

Hari Kishan Avasarala

Director and Chief Business officer

  • We look forward to your enquiries.
  • For APIs and Pharma Intermediates

Apurva Saphire, 87/2, III cross, Gottigere, BG Road, Bangalore-560083


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