Search result for FOOD AND DRUG ADMINISTRATION
40% of Pesticide Products in Nigeria are Banned by the EU
The National Agency for Food and Drug Administration and Control (NAFDAC) in Nigeria has said that 40 percent of registered brands of pesticide products in Nigeria have been banned by the European Union and hence are harming people, animals, and the Nigerian environment.
Nigeria is a so...
JAPAN HEALTH MINISTRY REPORTS LESS THAN 1% OF PEOPLE HAD COVID-19 ANTIBODIES
Highlights –
- Japan Health Ministry reports less than 1% of people had COVID-19 antibodies.
- The govt. conducted tests of about 15,000 individuals at the end of 2020.
- Five prefectures participated in the antibodies test.
- In T...
THE U.S. FDA COULD SOON MAKE THE CORONA VIRUS VACCINE AVAILABLE
Highlights
- The move is not influenced by Trump administration
- It would be done only if the benefits outweigh the risks
The United States is observing the rising number of corona virus cases. To make the v...
REMDESIVIR APPROVED BY FDA FOR ALL HOSPITALISED COVID PATIENTS
Highlights:
• Remdesivir is now approved for all the hospitalized COVID positive patients
• Earlier on FDA has approved of blood plasma treatment too
Recently, CDC revised its guideline...
DR. SCOTT GOTTLIEB: A CHANGE IN THE REQUIREMENT FOR HOME CORONA VIRUS TESTS WILL PROVE HELPFUL
Highlights
- It would give faster results
- People can accordingly take the necessary precautions
Dr. Scott Gottlieb acknowledged the new move by the Food and Drug Administration. It could en...
TRUMP TO SIGN A DEAL FOR THE PURCHASE OF 150 MILLION RAPID CORONA VIRUS TESTS
Highlights
- It will cost around $5
- It delivers result in minutes
President Donald Trump is going to make a big announcement. It is regarding the purchase of 150 million rapid corona virus tests. The test is called the Bina...
DR. SCOTT GOTTLIEB: CONVALESCENT PLASMA TREATMENT MAY BE HELPFUL BUT NOT ENTIRELY EFFECTIVE
Highlights
- In the early stages of the outbreak, convalescent plasma was used to treat corona virus patients
- It was used on a case-by-case basis
To treat coronavirus patients, the Food and Drug Administrat...
PRESIDENT TRUMP LEFT SURPRISED ON THE FDA’S HOLD ON BLOOD TREATMENT THERAPY
Highlights
- Trump insists on its use if it proves to be good
- Health officials raise concerns about data on the treatment
On the emergency use authorization for convalescent plasma therapy, the Food and Drug Administration recently pla...
GILEAD COULD GET FDA APPROVAL FOR USE OF REMDESIVIR DESPITE MIXED TRIAL RESULTS
Highlights –
- Gilead could get FDA approval for use of Remdesivir despite mixed trail results.
- The FDA had approved in May for sale of the drug to be used on an emergency basis for patients with severe COVID-19.
- The company had publis...
DR. FAUCI: CORONA VIRUS VACCINE MAY NOT BE HIGHLY EFFECTIVE
Highlights
- The corona virus vaccine shall be at least 75% effective
- 50% or 60% effective vaccine would be considered as manageable
Scientists are working hard on the development of the vaccine for the corona virus. D...
SANTEN OBTAINS US FDA ACCEPTANCE OF PMA APPLICATION FOR DE-128
HIGHLIGHTS
- Santen Pharmaceutical Co., Ltd. has submitted the Premarket Approval (PMA) application for DE-128 (MicroShunt) for review.
- US FDA has accepted the application from Santen.
- DE-128 is an investigational surgical glaucoma implant.
Why we don't have an antibody for Lyme illness
Lyme sickness is the most widely recognized vector-borne ailment in the United States, contaminating a huge number of individuals every year. However there's right now no antibody available that can shield people from getting this malady — an answer that would be sought after in high-ha...
Pharma firm in Process of US Food and Drug Administration Approval for Type II Diabetes Clinical Trial
The pioneer in regenerative technologies, Global Institute of Stem Cell Therapy & Research also known as GIOSTAR, made an announcement saying that they are in the middle of getting approval from the US Food and Drug Administration for conducting type II diabetes clinical trials dedicated to d...
FDA Grants Orphan Drug Designation
APR Applied Pharma Research SA ("APR"), the Swiss pharma organization centered in specialty and uncommon restorative regions, declares that the US Food and Drug Administration (the "FDA") has conceded Orphan Drug Designation for its investigational tranquilize code-named APR-T...
FDA in Israel?
The nation of the United States has always been regarded as a great medical industry leader, and we think that the government might be continuing its high standards all over the globe and will be changing the whole pharmaceutical and drug industry pretty soon. The United States has been known for...
FDA over some drug
The drug industry of the nation of United States has been a prevalent one, and the world has been taking a liking to the way United states have handled the drugs and now also has started to hate it. The medications of the United States are defamed for their prices; some medicines have the costs t...
Cooling cap therapy
Around 70,000 of women succumb to cancer, according to the Indian Council of Scientific Studies, Tata Memorial Hospital has been incorporating this technology for the beyond two years on a tribulation foundation. The brand new scalp cooling treatment getting used at the side of chemotherapy is ap...
New electro modulation tech changing the medicine scene
The medical scene of the United States has seen significant changes as technology has been advancing and has been improving the medical scene. A new electric-based approach to medical treatments has been changing the view of the United States.
The use of neuromodulation in the medicine ...
Sanofi pulls histamine blockers from the U.S.
Sanofi pulls histamine blocker from U.S. and North American nation when matter found
The French drugmaker, same it was operating with health authorities to work out the extent and extent of the recall, that known as is named is termed a preventative life being taken thanks to potential ...
Pharmas recall products citing contamination concerns
Torrent pharmaceuticals are a huge and well-recognized name in the United States market despite being a company based in India. The pharmaceutical firm has been long in the game in the United States market and has a good hold over the clients.
Not a long time ago some pharmaceutical compan...