Havix Group

Aavis Pharmaceuticals is respected for having acquired strong capabilities for developing generic formulations and world class generic products over the years. Aavis Pharmaceuticals is a USFDA approved, privately owned and one of the fastest growing pharmaceutical company based out of Atlanta Region, USA.

We recognize that Research and Development is vital for our survival and growth as a specialty pharmaceutical company thus Aavis mainly focuses on research and development of immediate release and controlled release oral solid that are complex in nature and present competitive barriers to entry. The breadth of the Company's technology platforms enables it to have more than one solution for any drug formulation challenge.

We have partnered with global contract manufacturing company with distinct distribution network and effective sales team and are constantly focusing on exploration and identification of business opportunities to partner with other companies globally, for in-licensing of products that are in accordance with the Company's strategic goals.

Aavis Pharmaceuticals is respected for having acquired strong capabilities for developing generic formulations and world class generic products over the years.

Develop and implement drug manufacturing safety guidelines and monitor product quality to ensure compliance standard and specifications with cGMP/GLP, ANDA, and 21CFR; Provide QA support for solid dosage; Review and ensure compliance of test results; Review Master Batch Records/Executed Batch Records, Change Controls; Review and approve technical documents (Process Validation, Equipment & Facility Validation), IPQA, CAPAs, SOPs, deviations, OOS, Handling of DEA documents, Provide support for all regulatory audits, internal/external inspections, and other audits.