Pharmaceutical Industry Related Topics 
Electronic Health Reporter
SEPTEMBER 17, 2020
As many know, the pharmaceutical industry is heavily regulated and specialized, with slow drug-development timelines, strict processes and quality requirements, and rigid silos. The article The Impact of Agile In The Pharmaceutical Industry appeared first on electronichealthreporter.com.
Mobi Health News
AUGUST 5, 2020
The platform provides solutions in energy health and safety training and now brings its training expertise to the pharmaceuticals sector.
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Healthcare It News
MARCH 2, 2023
Sun Pharma probes cyber breach Indian pharma giant Sun Pharmaceutical Industries has reported an "information security incident," according to PTI. The news report noted that the company has already reported the incident to the authorities and has since isolated its affected IT assets.
HIT Consultant
OCTOBER 25, 2022
Michael Galarnyk, AI Evangelist at cnvrg.io. The costs for drug discovery and development are skyrocketing, but AI (artificial intelligence) is introducing new efficiencies to help find effective treatments faster. A study in 2020 concluded that the estimated median capitalized research and development cost per product was $985 million.
Dot Compliance
MAY 3, 2024
In the pharmaceutical industry, the importance of regulatory compliance extends beyond fulfilling legal obligations. Compliance can be streamlined with the help of an electronic quality management system (eQMS) that incorporates regulatory standards into every operational aspect of a pharmaceutical organization.
Dot Compliance
OCTOBER 11, 2024
A good CAPA system is critical to the pharmaceutical industry. Regulatory Compliance Adherence to regulatory requirements, such as those outlined by the FDA’s 21 CFR Part 820, is mandatory for pharmaceutical manufacturers. The post What is CAPA in the Pharmaceutical Industry? What’s the Big Deal about CAPA?
Dot Compliance
OCTOBER 11, 2024
A good CAPA system is critical to the pharmaceutical industry. Regulatory Compliance Adherence to regulatory requirements, such as those outlined by the FDA’s 21 CFR Part 820, is mandatory for pharmaceutical manufacturers. The post What is CAPA in the Pharmaceutical Industry? What’s the Big Deal about CAPA?
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