Due to more complex supply chains, policy makers worldwide are enforcing stricter regulations for manufacturing and logistics.
Selected manufacturing problems and growing public pressure have caused the US Food and Drug Administration (FDA) to strengthen GMP standards (Good Manufacturing Practices) and control them more strictly.
Within a decade, the number of FDA warning letters sent to medical device manufacturers has increased threefold, from 61 letters in 2002 to 181 in 2012 (EC A 2012).
The number of FDA inspections of drug and biologics manufacturers has also grown. In the years to come, the FDA expects domestic GMP inspections to decrease and more inspections in the foreign arena (FDA 2013) reflecting the trend towards more globalized supply chains.
The Top Ten Trends Transforming the Pharmaceutical Supply Chain
The pharmaceutical landscape continues to morph at a rapid pace, and participating companies are having to develop ever more sophisticated supply chain processes and strategies in order to deal with ongoing changes in demographics, urban migration, increasing demand for healthcare, shifts toward age related disease patterns, and a rising health awareness across the population. This paper explores the top 10 trends that are transforming the pharmaceutical supply chain. Download the White Paper if you want to learn about:
At the same time, most emerging countries themselves are increasing their regulatory requirements. China published new GMP guidelines in 2012 and called on pharmaceutical companies to pursue GMP certification by the end of 2013.
Hand in hand with GMP standards, governments and international organizations such as WHO, have established and increased their requirements for Good Distribution Practices (GDP) – these standards define how life sciences products, particularly pharmaceuticals, have to be stored, transported and handled.
Higher GDP standards are looming in a number of countries – new guidelines will come into force during 2014 in Brazil, the European Union and China. Singapore is currently drafting new GDP standards (ColdChainIQPC).
Key new requirements in the European Union include risk assessment of delivery routes, temperature monitoring and reporting of temperature excursions and the use of dedicated vehicles where possible.
Challenges for the life sciences industry will have many consequences for logistics within the sector. Shifting disease patterns and innovative products will have an impact on what and how we store and transport.
Regulation, competition and cost pressure will have a direct affect logistics procedures.
Market changes and decentralized supply chains will require new and modified transportation routes.