Medtech Insight is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

UK region nears 100% LBC screening

This article was originally published in Clinica

Executive Summary

285,000 (75%) of the 380,000 screens performed annually in the UK's West Midlands region of the NHS use liquid-based cytology (LBC). So said Hologic this week, reporting that nine of the region's 13 screening programmes have now converted from traditional Pap smear screening to LBC ThinPrep Pap Test, developed by Cytyc. "Substantial parts" of another two regions have also converted. The 13 programmes operate through 11 laboratories. All UK women aged 25-64 years are routinely invited for screening once every three years up to the age of 50, and then every five years. Cytyc became a wholly-owned subsidiary of Hologic in October 2007, in a $6.2bn merger (see Clinica No 1279, p 15).

You may also be interested in...



Partisan Politics Returns To US FDA Congressional Oversight

The US FDA has stood out as an agency that tends to draw broad bipartisan support amid a generally rancorous and divided Congress. A House hearing, however, may be a sign that those days are over.

GLP-1 Coverage Restrictions In Medicare Part D Surge As Demand For Obesity Drugs Grows

A major shift from unfettered coverage to prior authorizations was recorded by MMIT over the past year for the leading GLP-1/GIP agonist diabetes drugs. Public interest in using the drugs off label for weight loss drove the change.

Roche Gets Adjuvant ALK+ Lung Cancer To Itself With Alecensa Approval

The US FDA cleared Roche’s supplemental approval request for ALK inhibitor Alecensa in ALK-positive non-small cell lung cancer following tumor resection.

Topics

Latest Headlines
See All
UsernamePublicRestriction

Register

MT046027

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel