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What’s next for Container Closure Integrity Testing?

Pharmaceutical Technology

A vitally important assay used across various stages of drug development and manufacturing, container closure integrity testing (CCIT) involves evaluating packaging systems to determine their ability to protect the stability and sterility of pharmaceutical products. The evolution of CCIT. Many test methods have thus been developed.

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A winning combination: The benefits of micronization and containment in a single installation

Pharmaceutical Technology

This, coupled with small pharma companies being unable to acquire or access containment capabilities in-house, means that the demand for innovative specialized small molecule capabilities remains high. Of those, only 935 (34%) small molecule API facilities offered some type of containment capabilities.

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Container Closure Integrity Testing (CCIT): How to get started with deterministic methods

Pharmaceutical Technology

With the new version of EU GMP Annex 1 coming into effect on 25 August this year, big changes to the way the pharmaceutical industry approaches container closure integrity testing (CCIT) are in motion. In addition, 100% testing is now required for fusion-sealed containers such as ampoules and IV bags.

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Leading pharmaceutical benefit managers and management companies

Pharmaceutical Technology

The list includes companies that offer various benefit management services, including but not limited to: · Regulatory compliance. The document contains detailed information on the suppliers and their product offerings, alongside contact details to aid your hiring decision. Health intelligence and analytics.

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AI-Powered Precision Engagement in Commercial and Medical Functions

Intouch Solutions

Instead, it will be a transformational process that affects various functions of the organization, triggering considerations related to data privacy and security, regulatory compliance, and change management. Facilitating cost containment and expediting the content approval process in accordance with regulatory compliance.

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Rising demand for pediatric dosage forms requires reformulation, expertise, and to-scale manufacturing capabilities

Pharmaceutical Technology

Formulation decisions made in the development of PDFs can have important implications for drug stability, patient compliance, and accurate dosing. A frequent example of a client challenge is the growing trend in which pharma companies are combining two or even three APIs in one formulation.

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Keeping tabs on Covid-19: Thermo Fisher Scientific antibody test is granted the CE Mark Certification and pharma cargo companies prepare for temperature-controlled vaccine delivery

The Pharma Data

SeaCube Containers , a pharmaceutical cargo trade company, has acquired 200 storage containers developed by Carrier and Sensitech to help address the anticipated increase in demand for refrigerated storage capacity and cargo visibility in support of Covid-19 vaccine distribution.