AVASAR offers top-notch, customer-focussed solutions that set us apart in quality, cost-effectiveness and reliability. Your trust is important to us.
Read moreAs 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.
Read moreGMP audits
Audit Standard applied
Updated- Dec 25
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.
Read moreThe Active Drug Substances (APIs) service ensures that our clients have access to a reliable and consistent supply of essential pharmaceutical ingredients.
Read moreWith our Pharma Intermediates service, you can count on reliable sourcing, consistent quality, and timely delivery to support your pharmaceutical manufacturing operations.
Read moreShare your requirements on mail id: A) asmurthy@avasarpharma.com -- For supplier qualification and GxP Audits B) sales@avasarpharma.com -- For API and pharma intermediates Contact: Mr.Murthy Phone: (+91) 9110714134 Working: Mon-Fri - 9.00 am - 5.30 pm


