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Searching Content by Indradeep Bhattacharya ordered by Published Date Descending.
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1
Protecting Your Trade Secrets In The UK
Trade secrets relate to valuable know-how and business information, that is undisclosed and intended to remain confidential.
UK
11 Jun 2019
2
Second Medical Use Patents In Europe: Are UK And Germany Swapping Approaches?
This White Paper defines "second medical use" claims and explains the "roles of intent" and "plausibility" in these infringement cases.
UK
10 Jan 2019
3
New French Decree Clarifies The Scope Of Biomedical Research
French Decree n° 2017-884 of May 9, 2017, was adopted to implement certain provisions of the Legal Ordinance of June 16, 2016, with respect to biomedical research.
France
4 Jul 2017
4
EMA Calls For Public Consultation On Clinical Trial Protocol
The EMA has opened for public consultation a draft guideline for the notification of serious breaches of the Clinical Trial Protocol (Regulation (EU) No 536/2014).
European Union
4 Jul 2017
5
Guidance For European MA Holders To Prepare For Brexit
The EMA has published a Q&A guidance for marketing authorization ("MA") holders of centrally authorized medicinal products to prepare for the United Kingdom's withdrawal from the European Union.
European Union
4 Jul 2017
6
FDA Reorganizes ORA Staff
The FDA envisions that these changes will result in a high level of technical expertise and more uniform application of the ORA's policies and processes.
United States
4 Jul 2017
7
Senators Urge The Administration To Certify Imports Of Prescription Drugs From Canada
This letter follows a previous request from February 14, 2017, that the same senators made to Secretary Price.
United States
4 Jul 2017
8
EMA Green Lights New EudraVigilance System For Adverse Reactions
The new and improved version of the EudraVigilance database will be launched on November 22, 2017.
European Union
4 Jul 2017
9
EU Medical Device Regulation 2017/745 And In Vitro Diagnostic Regulation 2017/746
Below is a high-level summary of some of the key changes brought by the MDR and IVDR to the regulatory framework applicable to medical devices.
European Union
4 Jul 2017
10
UK's Regulator Announces Its Top Priorities In The Lead Up To Brexit
The MHRA also announced a series of measures aimed at supporting innovation and improved access.
UK
15 May 2017
11
French ANSM Clarifies Guidance Related To Raw Materials For Pharmaceutical Use
Facilities located in France where RMPU is stored on behalf of distribution companies also fall within the scope of the authorization/declaration requirement.
France
15 May 2017
12
EMA Adopts A Guidance Concerning Periodic Safety Update Reports
The Explanatory Note addresses issues encountered by marketing authorization holders, and the Q&A is intended to help assessors evaluate PSURs in a consistent way.
European Union
15 May 2017
13
China's New Cybersecurity Law And Draft Data Localization Measures Expected To Burden Multinational Companies
Companies should take careful note of this new privacy and cybersecurity landscape to ensure their business practices align with legal and regulatory requirements.
China
15 May 2017
14
Update On Recommendations And Initiatives Of EU Regulators Ahead Of Brexit
On April 27, 2017, the EMA held a meeting with the heads of the National Competent Authorities of the EU/European Economic Area Member States to discuss the consequences of Brexit...
European Union
12 May 2017
15
Senate Confirms Dr. Gottlieb's Nomination As FDA Commissioner
On May 9, 2017, the Senate confirmed Dr. Scott Gottlieb as the next FDA commissioner. With a 57-42 vote, the Senate fills the commissioner position most recently held by Dr. Robert Califf...
United States
12 May 2017
16
New York Attorney General Announces Settlements With Three Mobile Health Application Developers
New York has made a mark on the regulatory and enforcement landscape for mobile health applications with the New York Attorney General's March 23, 2017, announcement of settlements...
United States
12 May 2017
17
Balancing The Scales — The Emerging European Approach To Tackling IP Issues In The Online World
Due to the influence of the internet, the last two decades have dramatically reshaped how business is conducted and how content is produced, distributed, and consumed.
European Union
26 Jan 2017
18
Fifty Shades Of Criminal Liability: "Grey" Goods And Beyond
The recent Court of Appeal decision in R v C and Others confirms that dealings in certain types of "grey" goods may be potentially subject to criminal sanctions in the same way as counterfeit goods.
UK
7 Dec 2016
19
欧洲商标法改革综述
继马克斯-普朗克知识产权与竞争法研究所发表《关于欧洲商标体系总体功能的研究》及欧盟委员会采纳其建议后,欧洲议会于2015年12月批准了对É
European Union
13 Jul 2016
20
Overview Of European Trade Mark Law Reforms
This Commentary highlights some of the most significant changes that will be made to the European trade marks regime as a result of the EUTMR and EUTMD which we believe are most relevant to our clients and friends.
European Union
10 Apr 2016
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