Facility

State-of-the-art infrastructure ensuring quality and compliance

Our Manufacturing Excellence

01

Three cGMP Facilities

Cerata Pharmaceuticals LLP operates three independent cGMP-compliant API manufacturing facilities with a combined installed capacity exceeding 100 metric tons, dedicated to the manufacturing of Steroid & Hormone, Oncology, and Peptide Active Pharmaceutical Ingredients.

02

Global Production & Export

We produce 100s of tons of APIs annually, exporting to over 40 countries and consistently meeting global pharmaceutical needs.

03

Global Quality Standards

We maintain strict global quality standards, delivering uniform product quality and reliability across all markets. Our facilities are approved by leading regulatory authorities and are trusted by Big Pharma and multinational companies worldwide.

Our Manufacturing Facility

State-of-the-Art Infrastructure

Advanced cGMP compliant facilities

Accreditations & Certifications

Our commitment to quality is validated by global regulatory approvals and certifications

WHO GMP Certification

WHO GMP Certified

Meeting World Health Organization Good Manufacturing Practice standards

DUNS Registered

DUNS Registered

Globally recognized business identification and verification

Our Core Capabilities

Hormones & Steroids

Comprehensive hormone and steroid API manufacturing with advanced synthesis techniques.

Oncology

Specialized oncology API manufacturing with advanced synthesis techniques and targeted therapies.

Peptides

Peptide API manufacturing using cutting-edge technology for complex molecular structures.

Key Facility Features

cGMP compliant manufacturing facilities
Regulatory approvals from global authorities
Advanced process equipment and technology
Strict quality control and assurance systems
Environmentally sustainable operations
Skilled workforce with technical expertise