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Latest From Philips Healthcare
2017 was another record year for novel device approvals in the US, with typical large numbers of cardiovascular and IVD go-aheads, along with notable successes in neurology, with noninvasive stimulation and digital-app solutions seeing success. There was also an increase in 510(k) clearances last year. Here's a look at some key FDA approvals and clearance trends from the past year, including in infographic form.
2017 proved to be a busy year for medtech M&A activity, with the number of deals rising from 174 in 2016, to 206 in 2017. The year also brought a number of notable acquisitions, including Becton Dickinson's blockbuster $24bn purchase of CR Bard and Dutch health-care giant Philips undertaking an ambitious acquisition spree. Medtech Insight takes a look at the highlights of 2017 and what's in store for 2018.
FDA’s expectation is that the most responsible individual at manufacturing sites be involved in inspections. The agency is increasingly talking about its “responsible corporate official” or Park Doctrine powers to hold top officials responsible for manufacturing issues and problems.
Protecting Against Individual Prosecutions: Execs Remain A Focus, But There Are Ways To Reduce Risks
As the US Justice Department continues its focus on individual liability in device industry enforcement, it’s more important than ever that manufacturers bring executives in early on problems to limit liability.
Diagnostic Imaging Equipment & Supplies
- MRI, NMR
- Monitoring Equipment & Devices
- Diagnostic Imaging Equipment & Supplies
- Therapeutic Areas
- Philips Medical Systems Inc.
- North America
- Parent & Subsidiaries
- Royal Philips Electronics NV
- Senior Management
Deborah DiSanzo, EVP, CEO
Abhijit Bhattacharya, EVP, CFO
- Contact Info
Phone: (978) 659-3000
3000 Minuteman Rd.
Andover, MA 01810-1099
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