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By World Courier

Content Provided by World Courier

The move from cold-chain to temperature-controlled shipping

World Courier shares an overview of the key issues and new developments in temperature-controlled shipping. 

By Reading Scientific Services Ltd.

Content Provided by Reading Scientific Services Ltd.

Extractables and leachables analysis of pharmaceutical products

A crucial undertaking when releasing pharmaceutical products for the market, is to determine the purity of the final product, necessitating the need to determine its impurity profile. Traditionally, this was concerned only with those impurities arising from the manufacture and degradation of the pharmaceutical product.  Nowadays, migration of mobile chemical species from components used in the manufacture and storage of pharmaceutical products must be assessed.

By Reading Scientific Services Ltd.

Content Provided by Reading Scientific Services Ltd.

Cleaning Validation - What do you need to consider to ensure a successful outcome?

Cross contamination must be avoided in the pharmaceutical industry at all costs. Successful cleaning validation ensures that patients are not put at risk due to cross contamination. The process can be divided into a number of sections each of which must be fully understood. Areas of concern must be addressed to ensure a successful outcome across the entire process. 

By World Courier

Content Provided by World Courier

The logistics link in successful cell and gene therapy trials

World Courier shares how logistics can make or break a cell or gene therapy trial.

By Recipharm AB

Content Provided by Recipharm AB

Developing a new high throughput screen method to improve excipient selection for solubilisation

A new high throughput screen method designed to improve the efficiency of testing excipients to solubilise compounds could save companies time, money and resource.

By World Courier

Content Provided by World Courier

Risk in global logistics: the top overlooked factors

World Courier shares an overview of the current risks inherent to the pharmaceutical supply chain in 2017.

By Covance Inc

Content Provided by Covance Inc

Investing in today’s CRA talent to ensure a stronger tomorrow

The importance of Clinical Research Associate training to support effective trials

By Reading Scientific Services Ltd.

Content Provided by Reading Scientific Services Ltd.

The impact of particles on pharmaceuticals

Sometimes it's the smallest details that have the biggest impact on pharmaceutical performance. That's certainly true when it comes down to the properties of particles and their impact on pharmaceutical performance. Subtle changes in particle size, shape and distribution can have a major impact on pharmaceutical solubility, stability and efficacy. 

By World Courier

Content Provided by World Courier

Clinical trials: World Courier explores opportunities in Southeast Asia

Southeast Asia is a growing pharmaceutical market, with a population of 620 million. What opportunities are there for multinational companies to access this rich area?

By World Courier

Content Provided by World Courier

World Courier discusses strategies for ensuring a successful supply chain

Once deficiencies in the supply chain are identified, how can the pharmaceutical industry ensure it manages product quality, consumer safety and organizational risk?

By Reading Scientific Services Ltd.

Content Provided by Reading Scientific Services Ltd.

The role of dissolution in drug development

Oral dosage forms remain one of the most flexible and effective treatments available to patients. Dissolution testing is a requirement for all solid oral dosage forms and is used throughout the development life-cycle for product release and stability testing. It is a pivotal analytical test used for detecting physical changes in an active pharmaceutical ingredient and formulated product

By World Courier

Content Provided by World Courier

World Courier discusses how healthcare, supply chain and public safety are inextricably linked

In globalising the pharmaceutical industry oversight and control has increasingly become a challenge in managing product quality, consumer safety and organisational risk.

By World Courier

Content Provided by World Courier

Discover what makes South Africa uniquely placed for running clinical trials in Africa

Down at the base of Africa is a country with amazing heritage, unique geography, and challenging patient populations. See why clinical trials happen in South Africa here

By Reading Scientific Services Ltd.

Content Provided by Reading Scientific Services Ltd.

Method development – why it matters to get it right

In an industry that is seeing increasing levels of outsourcing, the contract research organisation (CRO) needs to have proven experience in both the pragmatism and flexibility of method development and a regulatory background in validation.

By World Courier

Content Provided by World Courier

World Courier shares its insights on successful importation of clinical trial drugs into China

Getting a clinical trial drug into China is a complex business. Any discrepancies in paperwork or the physical shipment can lead to delays at customs or China Inspection & Quarantine. World Courier shares its experience for successful shipping.

By Reading Scientific Services Ltd.

Content Provided by Reading Scientific Services Ltd.

Impurity isolation and sample purification

During a manufacturing process unexpected and unknown impurities may arise in a sample. It is important that such impurities are isolated and identified.

By Catalent

Content Provided by Catalent

Demand led supply: A novel clinical supply approach tailored to today’s trials

The nature and scope of clinical research has changed significantly over the past decade. Studies are more complex, globalized and patient-centric than ever. Yet, the processes used to package and ship study drugs to trial sites are stuck in an earlier era, depriving sponsors of clinical supply models with the flexibility, speed and efficiency their programs demand. Now, that may be about to change with the advent of demand led supply (DLS), a clinical supply model tailored to today’s trials.

By Recipharm AB

Content Provided by Recipharm AB

Take steps to stay in the serialization race

As the deadline for drug serialization in the EU looms closer, it’s time to put the topic firmly on your agenda. Learn how to overcome the serialization challenge and simplify compliance.

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