Get a Quote
Get a Quote
Wide shot of a sterile pharmaceutical cleanroom with automated packaging lines and stainless steel vessels under bright fluorescent ceiling lighting
Wide shot of a sterile pharmaceutical cleanroom with automated packaging lines and stainless steel vessels under bright fluorescent ceiling lighting
Manufacturing Infrastructure

Certified Formulations

Dual Manufacturing Divisions and Approved Facilities

Altarsri Labs delivers high-throughput manufacturing across dedicated human healthcare and veterinary pharmaceutical wings, backed by validated cleanroom infrastructure and regulatory licenses.

Close-up of blister packaging line sealing pharmaceutical tablets in cleanroom conditions with automated inspection cameras
Close-up of blister packaging line sealing pharmaceutical tablets in cleanroom conditions with automated inspection cameras
Automated rotary tablet press manufacturing large veterinary boluses in a sealed sanitary industrial suite
Automated rotary tablet press manufacturing large veterinary boluses in a sealed sanitary industrial suite
Human Product Range
Veterinary Catalogue

Core Capabilities

Dedicated Processing Facilities

Human Pharmaceutical Manufacturing

Segregated production blocks engineered for Beta-Lactam and Non-Beta-Lactam tablets, oral dry syrups, liquid suspensions, and hard gelatin capsules adhering to strict therapeutic bioequivalence.

Veterinary Medicine Formulations

Purpose-built veterinary wings providing large-scale bolus compression, therapeutic dry syrups, and veterinary liquid supplements designed specifically for livestock and companion health.

Quality Accreditations

Verified Regulatory Approval List

Every batch produced across our human and veterinary wings complies with documented pharmacopeial monographs, verified through accredited national and international quality frameworks.

GMP Certification

Drug Controller Licensing

ISO 9001:2015 Quality Systems

GLP Certified Quality Control

Audited compliance ensuring continuous HEPA filtration, HVAC temperature-humidity mapping, and validated computerized clean-in-place sanitization protocols.

Comprehensive Schedule M clearances granted by state drug licensing authorities for non-sterile and oral solid dosage forms.

Standardized analytical documentation, complete raw material vendor qualification, and end-to-end computerized batch tracking.

In-house analytical instrumentation including HPLC, dissolution testers, and microbial incubation suites ensuring absolute potency.