07006552935 info@bharatsterile.com Mon–Sat: 9:00 AM – 6:00 PM IST

Warehouse

GMP-compliant storage solutions with real-time monitoring for raw materials and finished sterile APIs.

How We Manage Our Warehouse

Our warehouse operations are governed by strict GMP guidelines to ensure the integrity, identity, and quality of all materials stored — from incoming raw materials to finished sterile APIs awaiting dispatch.

  • 1
    Controlled Storage Conditions

    Dedicated storage zones for ambient (15–25°C), cool (2–8°C), and controlled room temperature materials, with continuous temperature and humidity monitoring logged to a central system.

  • 2
    Quarantine and Release Protocol

    All incoming materials are placed in dedicated quarantine zones until QC testing is completed and QA approval is given. No material is issued to production without formal release.

  • 3
    FEFO Inventory Management

    First Expired, First Out (FEFO) inventory management system ensures older materials are always used first, preventing expiry waste and maintaining material quality.

  • 4
    Traceability & Documentation

    Complete electronic and paper-based traceability for every material lot — from GRN through storage, issuance, and final batch reconciliation.

GMP pharmaceutical warehouse with controlled inventory management
Controlled pharmaceutical raw material handling and verification

Raw Material Handling Procedures

Every incoming raw material undergoes a systematic receiving and verification process before being approved for use in sterile API manufacturing:

  • 1
    Receiving Inspection

    Physical inspection of container condition, label verification, quantity checking, and documentation review against purchase orders and COAs from approved suppliers.

  • 2
    Sampling & QC Testing

    Representative sampling per approved sampling plans. Samples sent to QC laboratory for identity, purity, and quality testing per approved pharmacopeial or internal specifications.

  • 3
    Approved Vendor Control

    Only materials from AVL-approved suppliers are accepted. New suppliers undergo a formal qualification process before being added to the approved vendor list.

  • 4
    Storage and Issuance

    Materials stored in designated areas per storage requirements. Issued to production only against approved dispensing notes with dual verification.

Warehouse Features

Cold Chain Storage

Dedicated 2-8°C cold rooms and -20°C freezer storage for temperature-sensitive raw materials and APIs.

Real-Time Monitoring

Continuous temperature and humidity data logging with automated alerts for any excursions from defined limits.

Barcode Tracking

Each material lot is barcoded and tracked through all warehouse movements using an integrated inventory management system.

Controlled Access

Access-controlled zones for rejected, quarantine, and approved materials with CCTV surveillance throughout.

Segregated Storage

Complete physical segregation of raw materials, intermediates, finished products, packaging materials, and rejected items.

GMP Documentation

All warehouse activities are documented in GMP-compliant format with batch records and issuance logs maintained for regulatory review.

Warehouse & Logistics Enquiry

For storage specifications, cold chain capabilities, or material dispatch enquiries.