Mondaq All Regions: Food, Drugs, Healthcare, Life Sciences > Life Sciences, Biotechnology & Nanotechnology
Dentons
Advertisers are reminded the Therapeutic Goods Advertising Code 2018 (TGAC) was recently amended by the Therapeutic Goods Amendment (Therapeutic Goods Advertising Code) Instrument 2019.
DLA Piper
DLA Piper is pleased to launch Brexit: The Implications for the Life Sciences Sector, an interactive guide designed to help companies in the sector navigate Brexit.
Cyril Amarchand Mangaldas
Gujarat has been the flag bearer of India's pharmaceutical industry since the establishment of the country's second oldest drug company
S.S. Rana & Co. Advocates
A counterfeit product is one that is intended to deceive consumers into buying a fake or fraudulent product by misappropriating someone else's registered trademark or one that is deceptively similar
Khurana and Khurana
IIPRD has been successfully conducting several symposiums over the years on different Intellectual Property (IP) aspects.
Nishith Desai Associates
Regulation of medical devices has speedily evolved in the preceding two years. Before the introduction of the Medical Device Rules, 2017 ("MDR 2017"), the regulation of medical devices
STA Law Firm
The Ministry of Commerce and Industry (the MoCI) in Oman has resolved the implementation of the GSO 1943/2016 (the specification).
Gün + Partners
(A) Are there any special requirements, by way of law of practice, for technical and organisational measures
Morrison & Foerster LLP
We are pleased to announce the launch of the MoFo NDCal IP Resource Center. This complimentary resource is available to the public and provides insights on the judges
Reed Smith
Few things raise our blood pressure as much as the MDL process. MDL stands for Multi-District Litigation, but the M might as well stand for Mutilating and the D for Distorting.
Foley & Lardner
In a non-precedential opinion, the Federal Circuit held as patent-ineligible patent claims to personalized therapy to treat patients who would benefit from inhaled nitric oxide treatment
BakerHostetler
FDA Issues Reminder to Firms Exporting Collagen, Gelatin or Seafood Products – The FDA reminded exporters to the European Union to use the Export Listing Module (ELM) when exporting food products
Hogan Lovells
On 6 September 2019 the U.S. Food and Drug Administration (FDA or the agency) issued its final guidance document entitled "Humanitarian Device Exemption (HDE) Program."
Reed Smith
We had been waiting for the Utah Supreme Court's decision in Burningham v. Wright Medical for some time. As we pointed out in a blogpost when Burningham was first certified by the district court
Hogan Lovells
On 9 September 2019 the U.S. Food and Drug Administration (FDA or the agency) issued its final guidance document entitled "Acceptance Review for De Novo Classification Requests.
Oblon, McClelland, Maier & Neustadt, L.L.P
Claim 25 of Application No. 12/393,833, continued from the '803 application, also recited using random MPS to determine fetal aneuploidy.
Reed Smith
We've blogged numerous times about the tentative, non-final, and informal status of FDA warning letters (and untitled letters and similar enforcement precursors
Reed Smith
As your bloggers – at least those without school-aged children – begin to mourn the dawning end of summer, we do at least see one bright spot in the ever-shortening days
Ropes & Gray LLP
Tune in to this discussion to learn more about the expedited review programs and how to secure the benefits.
DLA Piper
The Therapeutic Goods Administration (TGA) has published a consultation paper seeking feedback on whether it should make excipient ingredients
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Oblon, McClelland, Maier & Neustadt, L.L.P
Design patents are very different from utility patents in that design patents only protect the ornamental features of an invention. In contrast to utility patents, the design is defined
McDermott Will & Emery
In April 2019, the US Food and Drug Administration (FDA) issued a white paper, "Proposed Regulatory Framework for Modifications to Artificial Intelligence/Machine Learning
Reed Smith
What follows is the second part of our extensive 50-state of cases precluding plaintiffs from proceeding with claims in the absence of admissible expert support. Part One was last week.
Cyril Amarchand Mangaldas
Gujarat has been the flag bearer of India's pharmaceutical industry since the establishment of the country's second oldest drug company
Torys LLP
Final amendments to the Patented Medicines Regulations have been announced by the Government of Canada giving the Patented Medicine Prices Review Board
Reed Smith
Because we didn't want to split Pennsylvania, this part is a little longer, and part two a little shorter, than average.
BakerHostetler
The 21st Century Cures Act (Cures Act), signed into law on Dec. 13, 2016, was designed to accelerate medical product development and bring new innovations
Ropes & Gray LLP
Third parties serve a critical function to multinational life sciences companies ("MNCs") internationally. MNCs rely on third parties for various functions
Withers LLP
The UK market for digital health solutions grew to £2.9 billion in 2018. Digital health systems represent the largest market both globally and in the UK
Esin Attorney Partnership
Türkiye İlaç ve Tıbbi Cihaz Kurumu ("TİTCK") 8 Ağustos 2019 tarihinde Kozmetik Yönetmeliği'nde ("Yönetmelik") değişiklik yapacağını duyurdu.
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