Zero-Tolerance Quality Policy

Purity, Potency & Standardized Safety

At Shikoy Pharma Pharmaceuticals Pvt. Ltd., quality is not a post-production inspection step; it is systematically verified into every stage—from active raw API selection at certified manufacturing units to robotic blister packaging and final batch dispatch.

Our WHO-GMP certified manufacturing partners utilize ultra-clean Class 10,000 & Class 100 HVAC air handling units (AHUs) with HEPA terminal filters, dedicated containment suites to eliminate cross-contamination, and fully automated sterile injection lines.

Advanced Analytical QC Suites

High-Performance Liquid Chromatography (HPLC), FTIR, and automatic dissolution testing.

Microbiological Sterility Validation

Bioburden profiling, environmental particulate air counts, and LAL endotoxin testing.

Stability-Controlled Blister Packaging

Alu-Alu tropical moisture barrier packaging preserving therapeutic active life up to 36 months.

WHO-GMP Accredited Partner Quality Testing Facility
Systematic Quality Architecture

4-Stage Zero-Defect Workflow

Our systematic quality management framework safeguards drug stability from chemical molecule stage to patient administration.

01
Raw API Assay

100% chromatographic identification and purity verification of active raw materials against Indian & British Pharmacopoeia.

02
In-Process Control

Continuous monitoring of tablet hardness, friability, disintegration time, fill-volume, and blend uniformity.

03
Finished Product QC

Automated dissolution profiling, stability testing in tropical walk-in chambers (Zone IVb), and microbial limits.

04
Batch Release QA

Formal Quality Assurance sign-off and issuance of certified Certificate of Analysis (COA) with each batch.

Accreditations

Global Quality Compliances

Every formulation released under the Shikoy Pharma brand adheres strictly to national and international pharmaceutical regulatory directives.

Browse Formulations
WHO-GMP

World Health Organization Good Manufacturing Practices Certification

ISO 9001:2015

International Quality Management System Validation

GLP Certified

Good Laboratory Practice for Analytical & Stability Integrity

DCGI Approved

Approved by Drug Controller General of India

Protection & Integrity

Specialized Packaging Standards

Our premium barrier packaging guarantees medicine potency, tamper-evidence, and protection against humidity throughout India.

Alu-Alu & Blister Foils

High-grade pharmaceutical aluminum foil seals out moisture, oxygen, and tropical heat, preventing tablet discoloration and degradation.

Amber PET & Glass Bottles

Shields oral liquid syrups and pediatric drops from photo-oxidation, complete with child-resistant measuring caps for exact dosage.

Aseptic Borosilicate Vials

Type-I neutral glass vials with bromobutyl rubber stoppers and tamper-evident flip-off seals for pyrogen-free injectable safety.

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