Search
Searching Content indexed under Food and Drugs Law by CMS Cameron McKenna Nabarro Olswang LLP ordered by Published Date Descending.
Links to Result pages
 
1 2  
>>Next
 
Title
Country
Organisation
Author
Date
1
More Cocoa Powder For The Swiss? The Swiss View On The "Nutella Gap"
Should Ferrero, the producer of Nutella, be hindered to produce a Swiss-style Nutella just for the Swiss market with more cocoa powder than the "normal" Nutella?
Switzerland
1 Mar 2018
3
New Trends: Reform To Drugs And Medical Devices In China
On 8 October 2017, the General Office of the State Council issued the Opinions on Deepening the Reform of the Evaluation and Approval System and Encouraging the Innovation of Drugs and Medical Devices.
China
9 Jan 2018
4
Upcoming CFDA Inspection On Class I And Class II Medical Devices Manufacturers
Circular (2014) No.15 provides for the specific deadlines for different domestic medical devices manufacturing companies to gradually meet the Medical Devices Manufacturing Quality Management Standards
China
9 Jan 2018
5
New Circular Further Enhancing The Development Of The Market Authorization Holder Regime
The China Food and Drug Administration ("CFDA") promulgated a new circular (2017) No.68 related to the promotion of a drug market authorization holder regime ("MAH Regime") work on 21 August 2017...
China
7 Jan 2018
6
New Clinical Trial Regime Will Substantially Speed Up Drug Registration Process In China
After receiving comments on the draft of the Decision of the State Administration of Food and Drug Administration on Adjusting the Relevant Issues Concerning the Registration and Administration...
China
20 Dec 2017
7
CFDA Seek Comments On The Amendments Of The Drug Administration Law Of The PRC
After the State Council issued the Opinions on Deepening the Reform of Examination and Approval System and Encouraging Innovation of Drugs and Medical Devices ("Opinions") on 8 October 2017, ...
China
12 Dec 2017
8
ECJ Ruling On Health Claims And Alcohol
A recent ruling of the European Court of Justice (Judgment in Case C-544/10 Deutsches Weintor eG v Land Rheinland-Pfalz) examined issues surrounding what constituted a health claim for a product under Health & Nutrition Claims Regulation 1924/2006 (NHCR).
UK
9 Oct 2012
9
New Blacklist System In The Field Of Pharmaceutical Security
Various blacklist systems are being implemented in a number of areas of Chinese administration, and from 1 October 2012 there will be a blacklist system in place for pharmaceutical security.
China
1 Oct 2012
10
New Legal Requirements: Labeling Of Food Products
EU Regulation 1169/2011 on the provision of food information to consumers, amending existing EU legislation on food and nutrition labeling, entered into force on 13 December 2011 (the "Regulation").
European Union
17 Sep 2012
11
Medical Device Manufacturers Risk Facing New Unannounced Inspections
On 18 June 2012, the State Food and Drug Administration ("SFDA") issued new regulations entitled "Interim Working Procedure of Unannounced Inspections over Manufacturing Enterprises of Medical Devices" ("Procedure").
UK
6 Aug 2012
12
Ban On Advertising Medicinal Properties Of Unregistered Products
Products which are not registered as medicines may not be advertised as having medicinal properties, according to a decision of the Chief Pharmaceutical Inspector.
Poland
6 Jun 2012
13
New Limits On Pharmaceutical Samples
From 1 January 2012, doctors will only be able to obtain a medicinal product sample for 2 years after first requesting it, and will be limited to a maximum of 4 samples per year.
Poland
4 Jan 2012
14
New Regulation In The Pharma Sector
On 5 December 2011 the Hungarian Parliament adopted a bill amending, inter alia, the Medicinal Thrift Act (Act No. XCVIII of 2006) and the Drug Act.
UK
16 Dec 2011
15
New Rules On Data Exclusivity Protection Of Original Pharmaceutical Products
The Parliament of Ukraine has recently adopted Law No. 3998-VI, introducing new rules to the Law of Ukraine on Pharmaceutical Products No. 123/96-ВР regarding data exclusivity protection of the original (innovative) pharmaceutical products registered in Ukraine.
UK
6 Dec 2011
16
New Regulations On Tax And Promotional Activities In The Pharma Sector
On 27 June 2011 the Hungarian Parliament adopted a bill amending, "inter alia", the Medicinal Thrift Act (Act No. XCVIII of 2006).
Hungary
5 Jul 2011
17
New Law On Reimbursement Of Pharmaceuticals
New laws governing the reimbursement of medicines, medical devices and foodstuffs for special medical purposes have been signed by the President.
Poland
31 May 2011
18
Pharmaceutical Inspectorate to Rule on Direct Drug Sales from Outside Poland
The Chief Pharmaceutical Inspector is entitled to supervise all pharmaceutical trade in Poland, including trade by companies based outside Poland, according to the Voivodship Administrative Court in Warsaw.
Poland
17 Nov 2010
19
Proposed Changes to Pharmaceutical Advertising
Significant proposed changes to pharmaceutical advertising are included in the ‘health pack’ currently being considered in Parliament.
Poland
1 Nov 2010
20
Extended Data Exclusivity Period for Pharmaceuticals
The data exclusivity period applicable to pharmaceuticals for human use is to be extended by the introduction of an 8+2+1 rule to replace the current 6-year exclusivity period.
Poland
27 Oct 2010
Links to Result pages
 
1 2  
>>Next