01

Session 1

Overview of Good Distribution Practice (cGDP) & regulations and framework

02

Session 2

Pharmaceutical Storage and Distribution Requirements

03

Session 3

Stores Design and Materials/Products Flow

04

Session 4

Materials Receipt, Quarantine, Release, and Storage

05

Session 5

Environmental Monitoring and Control

06

Session 6

Transportation

07

Session 7

Thermal Mapping and Qualification of Stores and Distribution Vehicles

08

Session 8

Pest and Rodents’ Control


09

Session 9

Products Distribution and Freight Forwarding

10

Session 10

ERP Systems in Pharmaceutical Distribution

11

Session 11

Supplier and Customer Approval, Vendor Management

12

Session 12

Reject Handling, Disposal, and Segregation

13

Session 13

Falsified Products

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In the pharmaceutical industry, it becomes imperative to observe the highest production and quality control standards to safeguard the efficacy and safety of medicinal products.
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