Current filters:  
Life Sciences, Biotechnology & Nanotechnology
China
DeHeng Law Offices
2020年1月30日,国家卫健委疾病预防控制局发布《预防新型冠状病毒感染的肺炎口罩使用指南》,明确口罩是预防呼吸道传染病的重要防线,可以ƀ
DeHeng Law Offices
随着新型冠状病毒肺炎疫情(以下简称"肺炎疫情")...
DeHeng Law Offices
新冠疫情肆虐,...
DeHeng Law Offices
自新型冠状病毒感染的疫情发生以来...
European Union
Reed Smith (Worldwide)
The Court of Justice of the European Union (CJEU) upheld decisions by the European Medicines Agency in two identical rulings on January 22, 2020.
India
Singh & Associates
On January 16, 2020, Indian Council of Medical Research announced a significant development that the WHO Global TB Programme has included an Indian Molecular assay...
Singh & Associates
The Central Drugs Standard Control Organization (CDSCO), New Delhi, under the aegis of the Ministry of Health ...
Mexico
OLIVARES
A decree was recently published modifying several provisions of the Health Law Regulations addressing the approval of biologic drugs.
Turkey
ELIG Gürkaynak Attorneys-at-Law
In May, 2019, the Agency had announced the Draft Regulation on Sales, Advertising and Promotion of Medical Devices, expected to replace the Regulation on Sales, Advertising and Promotion of Medical Devices, ...
United States
Foley & Lardner
How are businesses across the health care and life sciences spectrum collaborating to capitalize on the commercial promise of personalized medicine.
Reed Smith
This is a quick-hit post bringing you two first-of-their-kind orders on proving causation in cases alleging inadequate drug or medical device warnings.
BakerHostetler
FDA and CDC Announced the End of a Salmonella Outbreak in Fresh Fruit – The Food & Drug Administration (FDA) completed its investigation
Reed Smith
We've brought you some great news from the gadolinium contrast agent litigation last year and the hits just keeping on coming.
Reed Smith
We would be remiss (and out of character) if we plunged into a discussion of today's case without a shout-out to "Siba,"
BakerHostetler
FDA Announces Proposed Information Collections – The Notice "announces the FDA information collection request from the OMB for a generic clearance
Sheppard Mullin Richter & Hampton
The language of the FAR reflects an intent not to require "substantial transformation" for analysis under the FAR; "manufacture" does not require substantial transformation.
Sheppard Mullin Richter & Hampton
The core responsibilities of the FDA are to promote public health by reviewing and assuring the safety, effectiveness, quality, and security of drugs, vaccines, medical devices, and several other products.
Womble Bond Dickinson
If you believe there are important reasons to test your DNA, then ask your doctor to run the tests and explain the results.
BakerHostetler
The FDA "prepared this Small Entity Compliance Guide in accordance with section 212 of the Small Business Regulatory Enforcement Fairness Act (Public Law 104-121, as amended by Public Law 110-28).
Womble Bond Dickinson
So you want to know how much Neanderthal is in your genes.
FREE News Alerts
Sign Up for our free News Alerts - All the latest articles on your chosen topics condensed into a free bi-weekly email.
Popular Contributors
Upcoming Events
Tools
Font Size:
Translation
Mondaq Social Media