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N-FIS was developed to address a critical challenge in healthcare—needle phobia

Express Pharma

Key parameters, such as pressure and orifice size, are carefully calibrated to achieve accurate drug delivery at the desired depth and dosage, making it a safe and efficient alternative to traditional needle injections. Additionally, clinical trials have been conducted to validate the safety and performance of N-FIS.

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Pharmaceutical Continuous Manufacturing: Right for some products, but not all, and hurdles abound – workshop

Quality Matters

For certain drug substance and drug product manufacturing processes, PCM can bring opportunities to enhance flexibility and efficiency, lower production costs, cut environmental footprints, accelerate scale-up when needed, improve process control, and reduce potential quality issues, workshop participants reported.

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Romaco India opens solids processing experience centre in Hyderabad

Express Pharma

The Hyderabad centre is intended to cater to the needs of the Indian market, providing expert solutions for pharmaceutical, nutraceutical, and other industries dealing with solid dosage production. For more information or to send test materials, clients are encouraged to contact Romaco India at india@romaco.com.

Dosage 105
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Roquette opens pharmaceutical innovation facility in Pennsylvania, US

Pharmaceutical Technology

The facility complements the company’s current pharma innovation centres in France and Singapore, and intends to improve the patient experience with modern oral dosage forms. It also aims to contribute to the pharmaceutical sector by facilitating cross-industry partnerships and research-based product development.

Dosage 52
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Roquette opens new pharma innovation center in US

Express Pharma

With a focus on optimising patient experience with next-generation oral dosage forms, the US facility complements the cutting-edge research activities of Roquette’s existing pharma innovation centers in France and Singapore. Expert training, troubleshooting and scale-up advice will be priorities at the facility.

Dosage 52
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Paradigm Shift in Drug Development: Analytical Quality by Design and Analytical Procedure Life Cycle

Quality Matters

and increased complexity of the manufacturing process Traditional medicines have been evolving into more complex, sophisticated drug products, dosage forms, and advanced therapies. In parallel, manufacturing technologies (including adoption of artificial intelligence, advanced computing, etc.)

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How to conduct GMP training for employee

GMPSOP

GMP Points can be designed to be earned by the employees through attendance at internal and external GMP Training courses, workshops, certifications, etc. Product Overview: – Controlled drugs – Dosage forms – GMP – Applicable regulations – Introduction to the FDA c.