Blog
Why Management Reviews are Important
An element of a pharmacovigilance system is the Management Review, which is a systematic evaluation of the performance, ...
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Medicinal Product Recalls: What, Why and How
A medicinal product recall is a process of removing or correcting a defective or unsafe medicinal product from the marke...
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Warehouse Cleaning to GDP Standards
Warehouse cleaning is an essential part of maintaining good distribution practice (GDP) standards for the storage and tr...
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Data Integrity Compliance in GDP
Data integrity is the degree to which data is complete, consistent, accurate, trustworthy and reliable, and that these c...
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What is Quarantine in Good Distribution Practice?
According to the EU Guidelines on Good Distribution Practice of Medicinal Products for Human Use, it’s “…the status of s...
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GDP Transportation of Medicines
Medicines are highly sensitive products that require careful handling and storage throughout their supply chain, from th...
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CEIV Pharma IATA
The IATA CEIV Pharma certification (or IATA Centre of Excellence for Independent Validators in Pharmaceutical Logistics)...
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Temperature Control for Ambient Medicinal Product Storage
Temperature Control: Why is it important? Storing and transporting medicinal products at the right temperature is essent...
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What are GDP Guidelines for Medicinal products?
Good Distribution Practice (GDP) guidelines for medicinal products are a set of rules and recommendations that aim to en...
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Self-inspections (First-Party Audits)
These guidelines aim to ensure that the quality and integrity of medicines are maintained throughout the supply chain, f...
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How to be a Broker in Good Distribution Practice
Brokers are intermediaries who arrange transactions between buyers and sellers of medicinal products, but do not take ph...
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What is a WDA (H) (Wholesale Distribution Authorisation)?
The purpose of the requirement to hold a WDA (H) is to ensure that the regulations and guidelines relating to the procur...
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