Accreditations

International Quality & GMP Certifications

Farmers Pharma complies with the most stringent pharmaceutical manufacturing and quality control standards recognized globally.

WHO-GMP Certified
ISO 9001:2015 Certified
Schedule M Compliant
Annual Regulatory Audits
Our Certificates

Verified & Audited Accreditations

Each certification is maintained through rigorous annual audits and compliance monitoring.

WHO-GMP Certification
World Health Organization

WHO-GMP Certification

WHO-GMP

Our manufacturing unit has been audited and certified by WHO-GMP standards, ensuring every formulation is produced in a controlled, validated environment with full traceability.

Scope: Veterinary Pharmaceutical Manufacturing
Annually Renewed
ISO 9001:2015
Bureau of Indian Standards

ISO 9001:2015

ISO 9001

ISO 9001:2015 certification validates our quality management system — covering supplier qualification, process control, corrective actions, and management review.

Scope: Quality Management System
3-Year Certification
Manufacturing License
State Drug Authority

Manufacturing License

Mfg. License

Veterinary manufacturing license issued under Schedule M of the Drugs & Cosmetics Act, authorizing production of the full veterinary pharmaceutical portfolio.

Scope: Veterinary Product Manufacturing
Regulatory Compliance
Analytical Quality Compliance
In-House QC Laboratory

Analytical Quality Compliance

QC Lab

Certified in-house quality control laboratory equipped with HPLC, UV-Spectrophotometer, microbiology suite, and dissolution apparatus for full batch testing.

Scope: Pharmacopoeial Testing Standards
IP & BP Standards
Quality Standards

Why GMP Compliance Matters

Good Manufacturing Practice (GMP) certification ensures that products are consistently produced and controlled according to quality standards. For veterinary medicines, GMP means animal safety, farmer confidence, and regulatory acceptance.

  • Schedule M compliance for veterinary manufacturing
  • ICH-compliant stability testing protocols
  • Pharmacopoeial testing: IP, BP & USP references
  • Environmental monitoring of cleanrooms
  • Validated cleaning and sterilization procedures
  • Full batch records and document traceability

Certificate of Analysis Available

Every product batch comes with a Certificate of Analysis (CoA) documenting all quality parameters — assay, pH, sterility, microbial limits, and more.

Request batch-wise CoA
View regulatory submissions
Download product specifications
Request Documentation
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