Sirolimus (marketed as Rapamune) Information | FDA in Switzerland

     
aimmune receives positive chmp opinion on palforzia®

Aimmune Receives Positive CHMP Opinion on PALFORZIA®

Oct 16, 2020· LONDON, Oct. 16, 2020 (GLOBE NEWSWIRE) -- Aimmune Therapeutics, Inc., a Nestlé Health Science Company, today announced that the Committee for

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new drug approvals for 2019: synthesis and clinical

New drug approvals for 2019: Synthesis and clinical

May 22, 2020· By Alicia Ely Yamin. The shape of the COVID-19 pandemic and legal responses to it are changing rapidly across different contexts. Nonetheless, many of the issues raised in this global symposium will undoubtedly be the subject of scholarly and policy debates for the foreseeable future. Here I synthesize three emerging themes regarding structural challenges and democratic design.

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massachusetts man dies from eating too much black licorice

Massachusetts man dies from eating too much black licorice

Psilocybin studies in Europe. About a third of all experimental studies with psilocybin are happening in Europe. All of the European psychedelic research hubs – University of Zurich, University Hospital Basel and Imperial College London – are currently involved in clinical or

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the powerful run on mind medicine inc (otcmkts: mmedf

The Powerful Run on Mind Medicine Inc (OTCMKTS: MMEDF

Mind Medicine (MindMed) Inc (OTCMKTS: MMEDF) is making a powerful move up the charts running into dollar land after the Company reported it has received approval of protocol design to evaluate microdoses of LSD for Adult ADHD in a Phase 2a

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cannabis in switzerland

Cannabis in Switzerland

Classification. Cannabis that contains more than 1.0% THC is classified as an illegal drug in Switzerland. Thus, according to the Federal Law on Drugs: the production, culture, use, and possession of cannabis, are all prohibited and considered as criminal infringements. These infringements are punishable by up to three years of imprisonment and/or a fine.

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preventing medication errors in the information age

Preventing medication errors in the information age

May 19, 2018· The United States and Europe are drugmakers' biggest markets, but just because a drug wins approval in one doesn't mean it will get the nod in the other.

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comparison of drug approval process in united states & europe

Comparison of Drug Approval Process in United States & Europe

CenterWatch provides a variety of clinical research products and services: including clinical trials and results, drug approvals, study grants, news and analysis, career and training opportunities for patients and professionals.

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nestlé completes acquisition of aimmune therapeutics swiss

Nestlé completes acquisition of Aimmune Therapeutics Swiss

Oct 14, 2020· Vevey, October 14, 2020 . Nestlé completes acquisition of Aimmune Therapeutics. Nestlé announced today the successful completion of its acquisition of

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cladribine

Cladribine

Cladribine, sold under the brand name Leustatin among others, is a medication used to treat hairy cell leukemia (HCL, leukemic reticuloendotheliosis), B-cell chronic lymphocytic leukemia and Relapsing-remitting Multiple Sclerosis (RRMS). Its chemical name is 2-chloro-2'-deoxyadenosine (2CdA). . As a purine analog, it is a synthetic chemotherapy agent that targets lymphocytes and selectively

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map of european countries that require the ce mark, ce marking

Map of European countries that require the CE Mark, CE Marking

The European Union comprises 28 countries that require CE Marking. Three additional countries (Norway, Iceland, Liechtenstein), although not officially part of the European Union, are signatories to the European Economic Area (EEA).

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nestlé completes acquisition of aimmune therapeutics swiss

Nestlé completes acquisition of Aimmune Therapeutics Swiss

Oct 14, 2020· Vevey, October 14, 2020 . Nestlé completes acquisition of Aimmune Therapeutics. Nestlé announced today the successful completion of its acquisition of

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moderna says covid-19 vaccine could be ready as soon as

Moderna Says COVID-19 Vaccine Could Be Ready As Soon As

Moderna says its COVID-19 vaccine could be ready for U.S. distribution as early as December. Speaking at a Wall Street Journal tech conference, CEO Stéphane Bancel said Moderna expects interim

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cladribine

Cladribine

Cladribine, sold under the brand name Leustatin among others, is a medication used to treat hairy cell leukemia (HCL, leukemic reticuloendotheliosis), B-cell chronic lymphocytic leukemia and Relapsing-remitting Multiple Sclerosis (RRMS). Its chemical name is 2-chloro-2'-deoxyadenosine (2CdA). . As a purine analog, it is a synthetic chemotherapy agent that targets lymphocytes and selectively

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covid-19 news: socialising at christmas poses ‘substantial

Covid-19 news: Socialising at Christmas poses ‘substantial

The worldwide covid-19 death toll has passed 1.35 million. The number of confirmed cases is more than 56.4 million, according to Johns Hopkins University, though the true number of cases will be

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what foods are banned in europe but not banned in the u.s

What Foods Are Banned in Europe but Not Banned in the U.S

The ONCOblot Test, which detects 27 cancers through a single blood test, will now be available in China, Taiwan, Hong Kong, Switzerland, Russia, Ukraine and Poland.

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map of european countries that require the ce mark, ce marking

Map of European countries that require the CE Mark, CE Marking

The European Union comprises 28 countries that require CE Marking. Three additional countries (Norway, Iceland, Liechtenstein), although not officially part of the European Union, are signatories to the European Economic Area (EEA).

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comparison of drug approval process in united states & europe

Comparison of Drug Approval Process in United States & Europe

In order to commercialize medical devices in the European Union, a CE Mark certificate is needed. This certification verifies that a device meets all regulatory requirements of the Medical Devices Directive (MDD), or Active Implantable Medical Device Directive (AIMD) as they apply to your product.

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rfa-fd-21-002: renewal-harmonization of technical

RFA-FD-21-002: Renewal-Harmonization of Technical

The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is a unique global association with the capability of bringing together pharmaceutical regulatory authorities and international pharmaceutical industry associations to harmonize scientific and technical aspects of drug registration.

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animal research achievements

Animal Research Achievements

Cancer deaths have been on a continuous decline in the United States since the 1990’s, but according to the American Cancer Society, there are still 1,658,370 new cancer cases and 589,430 cancer deaths in the U.S. each year.

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project management in the pharmaceutical industry | pmi

Project Management in the Pharmaceutical Industry | PMI

The discovery and development of the high blood pressure medication Vasotec®, a product developed by Merck Sharp & Dohme Research Laboratories (MSDRL) (West Point, PA, USA), demonstrates the achievements pharmaceutical companies can accomplish when they use project management practices and tools to realize projects. This article--comprising three smaller articles--examines the project

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accp education: 2020 accp virtual journal club november

ACCP Education: 2020 ACCP Virtual Journal Club November

Otito Frances Iwuchukwu, RPh, PhD (Moderator) Assistant Professor. Dr. Iwuchukwu is a Pharmacist Scientist who obtained her PhD in Pharmaceutical Sciences with specialization in Drug Metabolism and Pharmacokinetics/Medicinal Chemistry from Temple University School of Pharmacy in Philadelphia, Pennsylvania.

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