Zydus receives EIR for the transdermal manufacturing facility
This facility underwent an inspection from 15th to 19th July 2024 and has been classified as Voluntary Action Indicated
This facility underwent an inspection from 15th to 19th July 2024 and has been classified as Voluntary Action Indicated
Showcases specialty and sustainable materials for healthcare at Medtec China 2024
AMR poses a critical threat to global public health undermining decades of progress made in the field of modern medicine
The company will take all necessary steps to work with USFDA towards earliest remediation of the above facility
The partnership will provide health plans with an out-of-the-box compliance solution for CMS-9115 and CMS-0057 rules
Stringent regulatory environments can make OEMs reluctant to change processes and materials for approved medical devices
Finance Minister Nirmala Sitharaman is set to present the full budget for the current financial year on July 23
Enhanced collaboration under the Memorandum of Cooperation (MoC) between India and Japan in medical product regulations
New software solution helps manufacturers digitalize and gain insights from data to increase efficiency
Subscribe To Our Newsletter & Stay Updated