Mondaq Europe: Food, Drugs, Healthcare, Life Sciences
Elkington and Fife LLP
Following a Notice of the European Commission related to certain parts of the EU Biotech Directive (98/44/EC), the EPO has decided to stay all examination and opposition proceedings...
Arthur Cox
The new EU Medical Device Regulations were adopted by the European Parliament on 6 April 2017.
Jones Day
Facilities located in France where RMPU is stored on behalf of distribution companies also fall within the scope of the authorization/declaration requirement.
Jones Day
This certification process will replace the current approvals given by the Minister of Health.
Reed Smith (Worldwide)
In France, transparency requirements are regulated by two main sets of laws: "The French Anti-Gift Law" . . .
Reed Smith (Worldwide)
Article body Current Length: 9407 chars Long including spaces Source Preview The relationship between the life sciences industry and health-care practitioners is being reshaped in France through regulatory developments under both the French Anti-Gift Law and the French Sunshine Act.
Arthur Cox
On 4 April 2017, the Health Products Regulatory Authority ("HPRA") published for consultation a draft guide to distribution of medical devices and in vitro diagnostic medical devices.
Mason Hayes & Curran
The Government has been busy addressing three topical matters involving the sale of alcohol in Ireland.
Arthur Cox
The new EU Medical Device Regulations, which are due to be voted on by the European Parliament, will result in increased post market surveillance and vigilance requirements for medical device manufacturers.
Withers LLP
In occasione della conclusione di Vinitaly e a seguito dell`entrata in vigore del Testo Unico sul Vino (L. 12 dicembre 2016, n. 238), riteniamo utile esaminare le novità legislative e le iniziative a tutela del Made in Italy per il settore vinicolo.
Dentons
Il 1 aprile 2017 è entrata in vigore la Legge n. 24/2017 ("Legge Gelli") recante "Disposizioni in materia di sicurezza delle cure e della persona assistita, nonché in materia di responsabilità professionale degli esercenti le professioni sanitarie".
Mamo TCV Advocates
Following Brexit, the European Medicines Agency (EMA) will be forced to relocate its headquarters out of London. Several EU Member States have already expressed an interest in hosting the EMA.
ELIG, Attorneys-at-Law
On April 25th, 2017, the Ministry of Health ("Ministry") has published the Regulation on Packaging Information, Inserts and Tracking of Medicinal Products for Human Use ("Regulation") on the Official Gazette.
Moroğlu Arseven
Turkey has introduced new definitions and measurement specifications for food additives, in line with the European Union's approach.
Moroğlu Arseven
Turkey continues to make changes to food regulations in order to harmonize its approach with the European Union. New regulations introduce principles and procedures for adding vitamins, minerals and certain other items to foods.
Deloitte
This week I hosted a panel discussion on how we, as individuals approach health and wellbeing in the workplace and in our private lives.
Jones Day
The MHRA also announced a series of measures aimed at supporting innovation and improved access.
Mayer Brown
On May 2, the European Commission published a Notice to Marketing Authorisation Holders of Centrally Authorised Medicinal Products.
Pinsent Masons LLP
The UK has the potential to be a global leader in regenerative medicine, an expert has said.
Pinsent Masons LLP
New medical devices laws have been published in the EU's Official Journal.
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Deloitte
The pharmaceutical industry continues to face regulatory and reimbursement hurdles weighing on the research and development returns of pharmaceutical firms this year.
Deloitte
This week's blog by Amen Sanghera, an analyst here at the Centre, takes a deeper dive into 3D printing technology and its current and future uses across the healthcare and life sciences industry.
ELIG, Attorneys-at-Law
On April 25th, 2017, the Ministry of Health ("Ministry") has published the Regulation on Packaging Information, Inserts and Tracking of Medicinal Products for Human Use ("Regulation") on the Official Gazette.
Mayer Brown
On May 2, the European Commission published a Notice to Marketing Authorisation Holders of Centrally Authorised Medicinal Products.
Bishop and Sewell LLP
It is difficult to comprehend that you would ever lose the ability to manage your own affairs but mental and physical incapacity can happen to anyone at any time.
Egorov Pughinsky Afanasiev & Partners
In September 2016, the Antimonopoly Committee of Ukraine (the "AMC") handed down a significant decision holding a major global pharmaceutical company and its four Ukrainian distributors...
Reed Smith
This guest post – only our second post ever on European issues is brought to you by Reed Smith partners Marilyn Moberg and (in the UK) associate Bond, Kathryn Bond (sorry, couldn't resist).
Dehns
GlaxoSmithKline (GSK), one of the world's leading pharmaceutical companies, recently announced that it is adopting a new approach to patenting its products around the world with the aim of...
Deloitte
Since the UK voted to leave the European Union (EU), some eight months ago, the ongoing debate has been dominated by uncertainty - with limited guidance on how to plan for changes to come.
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