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Piper Alderman
The changes aim to simplify the requirements of the Code while continuing to promote accurate and balanced advertising.
After much anticipation in the industry, the regulatory amendments restoring access to restricted drugs under Health Canada's Special Access Program (the "SAP") finally came into force.
Notably, these changes do not guarantee that requests for access to psychedelic restricted drugs will be authorized.
Gowling WLG
On January 10, 2022, the Competition Bureau and Health Canada's Health Products and Food Branch (HPFB) issued a joint notice in support of a new intra-government alliance.
Areti Charidemou & Associates LLC
We would like to remind you that the Cyprus Tax Department had announced the submission deadlines with respect to the electronic declarations of withheld Special Defence Contribution and contributions to the General Healthcare System.
European Union
Ganado Advocates
On the 25 November 2021, in ‘Delfarma sp.zoo vs. Prezes Urzędu Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych', the Court of Justice of the European Union (the ‘‘CJEU'') ruled that the automatic expiration of a parallel import license of a medical product.
The new Regulations overhaul the EU regulatory framework for medical devices, improving clinical safety, traceability and market access for all manufacturers.
A parallel agreement was also secured with Medicines for Ireland ("MFI") on behalf of the generic and biosimilar industry in Ireland.
Arthur Cox
On 6 December 2021, the Irish Pharmaceutical Healthcare Association, the association representing the international originator biopharmaceutical industry in Ireland, published the finalised version of
After more than 10 years, the official standard of good manufacturing practices concerning medical devices has been updated. On December 20, 2021...
With the pandemic and its associated developments, the ability to timeously and efficiently place orders for drugs and medicine to meet the needs of patients and consumers has become crucial...
Esin Attorney Partnership
Türkiye İlaç ve Tıbbi Cihaz Kurumu ("Kurum") geçtiğimiz haftalarda (i) tıbbi cihazların test, kontrol ve kalibrasyonu, (ii) sahte, kaçak ya da yasal tedarik zinciri dışına çıkan ilaçlar, ...
Esin Attorney Partnership
The Turkish Pharmaceuticals and Medical Devices Authority (TİTCK) has published announcements regarding (i) testing, control and calibration of medical devices, ...
Çetinkaya Avukatlık Bürosu olarak temel odak alanlarımızdan biri olan sağlık hukuku ve uyumu konusunda sağlık sektöründe ulusal ve uluslararası pek çok paydaş ile iş birliği...
Moroglu Arseven
Guideline on Procurement and Use of Medicines from Abroad ("Guideline") was amended by the Turkish Medicines and Medical Devices Agency ("Agency")
Moroglu Arseven
Yurt Dışından İlaç Temini ve Kullanım Kılavuzu ("Kılavuz"), Türkiye İlaç ve Tıbbi Cihaz Kurumu ("Kurum") tarafından güncellenerek 23 Ekim 2021 tarihinde yayımlanmıştır.
Health and social care workers have been facing unprecedented pressures during the COVID-19 pandemic. The new wave of Omicron cases has swept across the UK causing staff shortages across the sector.
Fear of a "mental health crisis across the health and social care sector" in the UK has been expressed by Dr Talya Greene, the lead author of a Frontline COVID study report recently published in the European Journal of Psychotraumatology.
United States
Alston & Bird
Whether you are looking to enter the market or grow your footprint in the industry, you need to know what regulations are relevant and how to prepare to bring a dietary supplement to market.
Arnall Golden Gregory
In light of surging COVID-19 cases occasioned by the highly transmissible Omicron variant and questions from nursing homes regarding whether to limit visitation, the Centers for Medicare and Medicaid Services (CMS) ...
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