Nigeria's NAFDAC has mandated manufacturers of sachet alcohol and PET bottles under 200ml to recall their products or face facility closure, enforcing a nationwide ban.

The FDA has uncovered and busted a milk adulteration racket in Navi Mumbai, seizing 4,710 litres of suspect milk as part of the operation.

REGENXBIO's stock plummeted by 22% after the FDA placed a clinical hold on its RGX-121 gene therapy trial. The halt was due to a surprise finding, causing investor concern.

The FDA has suspended the licenses of restaurants located at the Mumbai Cricket Association and the Cricket Club of India due to reported hygiene issues.

BioCardia has announced that the FDA confirmed meeting minutes supporting a follow-on De Novo pre-submission for approval of its Helix Transendocardial Delivery Catheter.

The U.S. Food and Drug Administration (FDA) has accepted United Therapeutics' application for ralinepag, a drug intended for the treatment of Pulmonary Arterial Hypertension (PAH).

GSK's drug Jemperli has been granted priority review by the FDA for the treatment of rectal cancer.

Heranba Industries saw its shares gain 3% after reporting a rise in Q1 profit, while Aurobindo Pharma and Caplin Point Labs experienced declines due to USFDA-related issues.

A recall has been issued for frozen raw dog food after illnesses were linked to salmonella contamination. FDA testing found the bacteria in products shipped across 11 states.

Orum Therapeutics has announced that the U.S. FDA has cleared its Investigational New Drug (IND) application for ORM-1153, a novel CD123-GSPT1 degrader-antibody conjugate.

The Indian state of Karnataka has imposed a one-year ban on analogue paneer, with the FDA citing public health concerns as the reason for the prohibition.

A report indicates that lawmakers are calling on the FDA to scrutinize Chinese clinical trials following reports of deaths, raising concerns about research integrity and patient safety.

A new FDA-cleared tool has been introduced to combat lung cancer, which claims more women's lives than breast, ovarian, and cervical cancers combined, aiming to address individual nodules.

Ghana's Food and Drugs Authority (FDA) reported a GH¢70 million surplus in 2025, a 51% increase from the previous year, even as it faces operational challenges including aging laboratory equipment.

The Maharashtra FDA is focusing on edible oil quality, with official Mundhe flagging potential cancer risks and threatening stringent penalties for non-compliance.

Capricor's stock closed 58% higher after receiving what is described as an 'FDA lifeline,' prompting questions about the renewed prospects for product approval.

Jeffrey Tucker, founder and president of the Brownstone Institute, claims that top officials from the FDA and NIH informed him that the purpose of the COVID-19 lockdowns was to "delay the onset" of the pandemic.

IAS officer Tukaram Mundhe, known as 'Singham' for his strict approach, is back in the news for his rigorous enforcement against food safety violations as Maharashtra FDA Commissioner, reflecting his journey from a village school to a top UPSC rank.

Former President Trump has reportedly chosen Heidi Overton to head the Food and Drug Administration, according to Bloomberg News. This appointment would place her at the helm of the key regulatory agency.

Bud Leavell, a Parkinson's patient, experienced the disappearance of his years-long tremor within minutes of receiving an FDA-approved focused ultrasound treatment at UT Southwestern Medical Center in Arlington, Texas.

InspireMD has indicated potential FDA decisions in Q4 2026 and is targeting $9 million in annual cost savings.

The U.S. Food and Drug Administration has approved an autoinjector version of LEROCHOL® (lerodalcibep-liga) along with an updated indication for the drug.

The Food and Drugs Authority (FDA) has issued a warning to traders and the public about the unauthorized use of chemicals to accelerate plantain ripening, citing food safety concerns.

Aurobindo Pharma's manufacturing plant in Raleigh has been classified as 'Voluntary Action Indicated' by the US FDA.

The Maharashtra FDA has suspended Parle Agro's license after expired Frooti and Appy products were discovered in a Chembur godown.

The US FDA has raised the salmonella risk to the highest level for 19 million eggs, with nearly 100 people infected across 17 states and 26 hospitalized, though officials claim the situation is under control.

Restaurants in Maharashtra are rushing to address kitchen deficiencies with food safety experts following an FDA crackdown, while a KFC outlet in Mangaluru was shut down due to a food safety violation involving 'black chicken' and foul smell.

Nearly 1.6 million dozen eggs from Texas have been recalled across the US south and south-west due to a salmonella outbreak, elevated to the FDA's highest-risk warning.

Maharashtra FDA chief Tukaram Mundhe has indicated his consideration of entering electoral politics, discussing his potential move with media outlets.

The U.S. Food and Drug Administration has issued a recall for 19 million eggs, including 1.6 million dozen, due to potential Salmonella contamination. This recall has been classified under the FDA's highest risk level.

The recall was announced in July and impacted states including Texas, Oklahoma, Arkansas, Louisiana, New Mexico and Mississippi.

Nigeria's NAFDAC has retracted a previous alert regarding Deleject needles, stating that the products are now considered safe for use after an investigation into a complaint.

Tenon Medical has announced plans for sacropelvic product launches over the next six to nine months, following its recent FDA 510(k) clearance.

Despite assurances from the FDA that the parasite causing an explosive diarrhea outbreak has been removed from the food supply, cases of cyclosporiasis continue to rise, with nearly 25,000 reported across dozens of US states.

The US Food and Drug Administration has approved a feature for Samsung Electronics’ Galaxy Buds, allowing the earbuds to be used as over-the-counter hearing aids without requiring a prescription.

The Food and Drug Administration (FDA) has suspended the licenses of four Domino's and one Pizza Hut outlet in Mumbai, though the specific reasons were not detailed.

Since taking office three months ago, the Commissioner of the Food and Drug Administration (FDA) in India has reportedly put the state's food and beverage industry on edge, with past actions including raiding a court canteen and razing Dawood's 'palace'.

Dutch newspaper De Volkskrant reviews 'Los tigres', describing it as a thrilling yet somewhat excessive film with breathtaking underwater sequences.

RFK Jr. is advocating for greater FDA oversight of food ingredients, a proposal that could potentially cost $210 million.

The U.S. Food and Drug Administration (FDA) has proposed new regulations that would require food manufacturers to notify the agency before introducing new ingredients and additives into their products.

The Department of Health and Human Services (HHS) is taking steps to tighten oversight of food ingredients and define ultra-processed foods, responding to growing food safety concerns and questions about FDA visibility.

During checks by the Karnataka FDA, five hotels in Bengaluru were found to have unhygienic food, including meat with fungus and rotten vegetables. Food seized from Skyye lounge was deemed 'unfit for consumption' and discarded.

A multistate outbreak of Salmonella Javiana, which has sickened 345 people and impacted two restaurant chains, has been traced by the FDA to a single grower in Sinaloa, Mexico.

Cryoport, Apyx, and Consensus Cloud have all reaffirmed their 2026 revenue guidance, with Cryoport targeting $192M-$196M, Apyx $59.0M-$60.0M, and Consensus Cloud $350M-$364M. These companies are also outlining strategic expansions and adjusted EBITDA targets.

Nigeria's NAFDAC has issued a warning about suspected counterfeit asthma medication discovered in Eastern Nigeria, tracing it to a distributor's address in Anambra State.

The Food and Drug Administration (FDA) has ordered the closure of two canteens operating without proper licenses at IIT Bombay, while a third canteen received a notice.

Meryl Streep is auctioning off wardrobe pieces, including the iconic cerulean sweater, from 'The Devil Wears Prada 2' to benefit the CFDA and Committee to Protect Journalists.

Moderna's stock experienced a decline even after the company received a significant approval from the FDA.

The FDA has cleared a new freeze-dried plasma product for use, providing military medics with an additional life-saving blood care option closer to the point of injury for combat casualties.

The FDA has expanded its investigation into a Cyclospora outbreak linked to contaminated iceberg lettuce from Taylor Farms de Mexico, with confirmed cases now exceeding 6,000 across multiple states, resulting in 278 hospitalizations and two deaths.

The Maharashtra FDA Chief detailed methods of milk adulteration, including the use of products like shampoo, raising concerns about food safety.

The U.S. Food and Drug Administration is expected to decide whether to approve the first mRNA flu vaccine, a development that could mark a significant advancement in vaccine technology.

The FDA has permitted some Zyn nicotine pouches to be marketed as 'lower risk' than cigarettes, a decision public health experts believe could help smokers but raises concerns about potential addiction among young people.

The Maharashtra FDA Chief reacted strongly, calling the situation 'really disgusting,' regarding food licence cancellations following a viral video depicting unhygienic soya chaap preparation.

The FDA is under fire for allegedly prioritizing speed over safety in its approach to regulating peptides, raising concerns about potential health risks.

An FDA advisory panel recently voted to approve certain popular peptides, drawing considerable attention to their market. The decision has also sparked concerns regarding the currently unregulated supply of these products.

The Mumbai Confidential column reports on an internal test conducted by the Food and Drug Administration (FDA). Further details about the nature and outcome of the test were not provided in the snippet.

The U.S. Food and Drug Administration is evaluating Moderna's mRNA-based flu vaccine, which could be the first of its kind on the market, a decision expected to impact the biotech industry.

Hospitality organizations are urging authorities to withhold names and photos in response to a crackdown by the Food and Drug Administration.

The Food and Drug Administration (FDA) in Maharashtra, India, has issued a directive asking schools to cease the sale of junk food items popular among children.

The Food and Drug Administration (FDA) has stopped business at two canteens within the Bombay High Court premises, with the bar association stating the action was taken 'voluntarily'.

The U.S. Food and Drug Administration (FDA) has granted approval to Johnson & Johnson's drug Imaavy. This new treatment is approved for warm autoimmune hemolytic anemia, a rare blood disorder.

Capricor's stock has seen a rise after the FDA announced an extension to the action date for its drug Deramiocel.

Nigeria's National Agency for Food and Drug Administration and Control (NAFDAC) commenced a nationwide street-level crackdown on alcoholic beverages packaged in prohibited forms and targeting underage drinking.

Tempus has obtained FDA clearance for its artificial intelligence product designed for pulmonary hypertension.

Humacyte, a biotechnology company, is preparing to submit a filing to the U.S. Food and Drug Administration (FDA) in November for its dialysis access product.

A GSK drug has received approval in Japan, while Tracsis reports its trading performance is in line with expectations.

Heranba Industries reported a 3% gain in its Q1 profit, while Aurobindo Pharma and Caplin Point Labs saw their shares fall following observations from the USFDA.

The Saudi Food and Drug Authority (SFDA) has imposed fines totaling SR1.575 million on 17 pharmaceutical establishments for violations related to medicine availability and reporting.

Prestige Brand Holdings has voluntarily recalled approximately 40,000 bottles of its Clear Eyes eye drops across the US following an FDA alert regarding potential contamination and sterility issues.

The Maharashtra Food and Drug Administration (FDA) has suspended the operating licenses of a KFC outlet and Baba’s Kitchen in Pune due to identified food safety violations.

Philip Morris has obtained FDA approval for 11 new nicotine pouch products, expanding its portfolio in the nicotine market.

India's FDA has temporarily revoked licenses for several prominent establishments in Mumbai, including The Bombay Presidency Radio Club, Khar Gymkhana, and McDonald's Colaba, due to severe hygiene violations like poor waste management, pest control, and insect infestations.

The Food and Drugs Authority (FDA) in Ghana has processed more than 24,000 product applications in 2025. This indicates a high volume of regulatory activity for various products.

Implantica has secured FDA approval for its RefluxStop implant, designed to treat gastroesophageal reflux disease (GERD).

The FDA has elevated the recall of packaged frozen berries to a Class I warning, indicating the highest risk level. The affected fruits were distributed to Publix stores across eight states.

The Saudi Food and Drug Authority (SFDA) has granted marketing authorization for a new medical device that provides continuous, real-time monitoring of both blood glucose and ketones.

Strides Pharma Science shares rose sharply after the USFDA issued an Establishment Inspection Report (EIR) for its Bengaluru facility, concluding a recent cGMP inspection with five observations that the company addressed.

Senator Bill Cassidy, chairman of the Senate Health Panel, has voiced strong reservations about Dr. Heidi Overton, President Trump’s FDA nominee, citing her role in a recent executive order on vaccines as 'almost disqualifying.'

The Saudi Food and Drug Authority (SFDA) has stressed the importance of providing children with a balanced breakfast as schools across Saudi Arabia prepare to reopen for the new academic year on August 23.

Former President Trump has selected White House Health Adviser Heidi Overton to lead the FDA, following Marty Makary’s exit from the position.

The Maharashtra FDA chief has issued a warning to actors Shah Rukh Khan and Ajay Devgn regarding a notice concerning their endorsement of the Vimal brand, stating that action will be taken.

A discussion has emerged in Sweden regarding the country's five national minority languages, questioning whether immigrants should be able to learn languages like Pite Sami or Elfdalian as a path to Swedish citizenship.

The Maharashtra FDA chief has issued a stern warning, stating that 'no one will be spared' after notices were sent to prominent figures including Shah Rukh Khan, Ajay Devgn, and Tiger Shroff.

The FDA has proposed a new GRAS (Generally Recognized As Safe) rule aimed at addressing food ingredients that have never been reviewed, raising questions about its impact on food safety.

Quanterix is reshaping its sales strategy and is targeting a Q4 FDA decision for its Alzheimer's blood test, a key development for the company.

Eleven people, including children, fell ill in Maharashtra after a dead lizard was reportedly found inside a birthday cake, prompting a raid on the bakery by the FDA.

India's Food and Drug Administration (FDA) has requested explanations from actors Shah Rukh Khan, Ajay Devgn, and Tiger Shroff regarding their involvement in a Vimal Elaichi advertisement.

A Calgary-based company, Solvet, has received emergency FDA approval for its liquid ivermectin product for horses, which will be used to combat the growing risk posed by screwworm in the United States.

The Food and Drug Administration (FDA) has initiated a crackdown, taking action against 16 establishments, including prominent names like Burger King and Sayaji Hotel.

Nigeria's NAFDAC is enhancing its regulatory oversight of blood and blood products, classifying them as essential medicines that require consistent availability, quality, safety, and affordability.

NAFDAC and the Ogun State Police have strengthened their partnership to enforce the ban on sachet alcohol and small PET bottles, aiming to protect public health.

Restaurants and government canteens in Mumbai have voluntarily shut down for repairs and deep cleaning as the Food and Drug Administration (FDA) intensifies its crackdown on hygiene standards.

The U.S. Food and Drug Administration (FDA) has approved an mRNA flu vaccine, a development considered a major breakthrough in vaccine technology and public health. The new jab is expected to offer improved protection against influenza.

The Maharashtra FDA has issued notices to 135 Ayurvedic drug manufacturers and cancelled ten licenses due to unhygienic conditions, lack of technical staff, and inadequate raw material testing protocols.

Sweetgreen Inc. CEO Jonathan Neman stated that a cyclospora outbreak impacted the company's sales, though he noted the FDA has now deemed iceberg lettuce safe to eat and Sweetgreen's supply chain remains unaffected.

The Food and Drugs Authority (FDA) in Ghana has urged for enhanced measures to protect, promote, and support breastfeeding. This call was made as Ghana joined the global community in commemorating World Breastfeeding Week 2026.

Taysha Gene Therapies has outlined its REVEAL program's development schedule, anticipating a 6-month interim analysis and FDA feedback in the first half of 2027, with PPQ completion targeted for the fourth quarter of 2026.

The Food Safety and Drug Administration conducted inspections at Indira canteens in Bengaluru following reports of rats found in their kitchens.

RFK Jr. has introduced a new FDA proposal targeting 'unvetted' ingredients in the US food supply, aiming to address concerns about chronic diseases linked to American diets.

The US Food and Drug Administration (FDA) is proposing new rules for how food manufacturers notify them of ingredients, closing a loophole but not including a promised definition for 'ultra-processed' foods.

Johnson & Johnson's Ottava has received FDA approval, raising questions about its potential to challenge Intuitive Surgical in the medical device market.

A new plan for FDA Canal Road, proposing motorcycle segregation, improved service roads, and safer U-turns, is being questioned due to past failures in similar projects.

Saoji cuisine, a culinary legacy from Nagpur, is back in focus following a remark made by the FDA chief, prompting renewed interest in its unique flavors.

The Bombay High Court criticized the FDA for its action against Amazon Retail India's Bhiwandi warehouse, which was accused of sending expired food into the retail market instead of destroying it.

Praxis Therapeutics announced expectations for two FDA decisions within approximately six months and set a target of $10 billion in peak sales for its drug ulixacaltamide, alongside plans to build a 300-person field force.

The Maharashtra Food and Drug Administration (FDA) has banned non-dairy paneer, prompting experts to share important information with the public.

The U.S. Food and Drug Administration (FDA) has granted approval for Replimune's melanoma drug, marking a successful outcome after the company's third attempt to secure approval.

The U.S. Food and Drug Administration has approved Moderna's flu vaccine, leading to a significant increase in the company's stock value.

Roivant Chief Executive Officer Matt Gline expects the FDA to approve the launch of a new drug designed to combat a debilitating skin disease, with plans for it to be on the market by September.

Following a crackdown in Mumbai, the Pune FDA inspected 415 restaurants and suspended 43 licences, indicating increased regulatory action in the region.

The Bombay High Court has labeled the FDA's action as 'biased', a claim that Tukaram Mundhe, a prominent official, has vehemently denied, stating 'absolutely not'.

The U.S. Food and Drug Administration has given its approval for the first-ever mRNA-based influenza vaccine.

The U.S. Army's missile stockpile is dwindling and could take years to replenish. And, the Food and Drug Administration is deciding whether to approve a flu vaccine with mRNA technology.

The U.S. Food and Drug Administration is nearing a decision on whether to approve the first flu vaccine utilizing mRNA technology, similar to that used in COVID-19 vaccines. The development comes amidst ongoing public discourse, including skepticism from figures like Robert F. Kennedy Jr. regarding mRNA vaccines.

The FDA has approved a novel blood test for colon cancer, capable of detecting nearly eight out of 10 cancers. While convenient, experts note its limitations and question whether it will replace traditional colonoscopy, especially as colorectal cancer cases rise among younger adults.

The Lagos State Police Command has uncovered a suspected counterfeit pharmaceutical distribution network operating across Nigeria and West Africa, arresting two suspects and recovering large quantities of illicit drugs.

Bombay courts are frequently reversing instant restaurant closure orders issued by the Food and Drug Administration (FDA), indicating a trend of judicial oversight on regulatory actions.

FDA staff scientists are in opposition to an advisory panel's recommendation to ease access to compounded peptides, creating uncertainty about the agency's future actions.

Hotel associations in Maharashtra are urging Prime Minister Modi and Deputy Chief Minister Fadnavis to intervene following a crackdown by the state's Food and Drug Administration (FDA).

Nigeria's National Agency for Food and Drug Administration and Control (NAFDAC) has reiterated its commitment to maintaining the ban on small-volume alcoholic drinks sold in sachets across the country.

The US Food and Drug Administration has approved its first new sunscreen ingredient in decades, signaling potential opportunities for South Korea's K-beauty industry, though challenges remain.

The Bombay High Court canteen has temporarily halted its services following a visit by FDA officials, though the Bombay Bar Association stated the decision was voluntary.

Johnson & Johnson has received FDA priority review for its Rybrevant Faspro treatment, specifically for use in head and neck cancer, potentially accelerating its availability.

The U.S. Food and Drug Administration (FDA) has extended the PDUFA target action date for Capricor Therapeutics' Biologics License Application (BLA) for deramiocel to November 22. This extension allows the FDA more time to complete its review of the drug.

FDA chief Tukaram Mundhe has stated that he has not yet received a reply from Bollywood actors Shah Rukh Khan, Ajay Devgn, and Tiger Shroff regarding their endorsement of Vimal.

Avulux has been granted FDA De Novo Authorization, establishing the first lens classification specifically for migraine-associated light sensitivity.

Spruce Biosciences has successfully concluded its pre-Biologics License Application (BLA) meetings with the U.S. Food and Drug Administration (FDA) for its MPS IIIB therapy.

Filmmaker Kunal Kohli has publicly called upon FDA chief Tukaram Mundhe to conduct raids on Indian kitchens, expressing concerns about the prevalence of expired food items. His statement highlights issues of food safety and public health.

The Maharashtra FDA has initiated a crackdown on the sale of loose cooking oil, citing significant health risks and emphasizing the importance of verifying product purity for consumers.

Aurobindo Pharma's shares are under scrutiny after the USFDA issued an observation to its manufacturing unit located in Telangana.

Orum Therapeutics announced that the U.S. FDA has cleared its Investigational New Drug (IND) application for ORM-1153, a novel CD123-GSPT1 degrader-antibody conjugate.

The FDA has authorized ZYN ULTRA Nicotine Pouches following a scientific review, allowing the product to be marketed.

The injured were taken to the Sanjay Gandhi Memorial Hospital, with two of them later referred to the Safdarjung Hospital, police said.

The Taiwan Food and Drug Administration (FDA) has stated that recalled US berries, subject to a health alert, were not imported into Taiwan.

Ascelia Pharma's Q2 2026 slides indicate a significant FDA setback, delaying the development path for its drug Orviglance and making an upcoming FDA meeting crucial.

The Thai FDA has issued a statement recommending that 5,000 ppm fluoride toothpaste should only be used under expert guidance.

Ghana's Food and Drugs Authority (FDA) has reported a GH¢70 million surplus but also issued a warning about challenges related to laboratory equipment.

Ghana's Food and Drugs Authority (FDA) reported a GH¢70 million surplus in 2025, but highlighted aging laboratory equipment and the prevalence of illicit products as significant public health concerns.

United Spirits saw gains after the FSSAI revoked an order, while Glenmark Pharmaceuticals' shares rose following approval from the USFDA.

Regeneron has secured approval from the U.S. Food and Drug Administration (FDA) for its new therapy designed to treat a rare bone disorder.

Teva Pharmaceuticals has been granted priority review by the FDA for its new therapy aimed at treating Tourette syndrome, potentially accelerating its path to market.

Maharashtra Food and Drug Administration Commissioner Tukaram Munde defended the agency's action of imposing a ₹5 lakh fine on a Pune sweet shop, despite a Bombay Court order for compensation.

Tukaram Mundhe, an official, stated that Shah Rukh Khan, Ajay Devgn, and Tiger Shroff face a fine of up to ₹10 lakh if the FDA is unsatisfied with their explanation regarding the Vimal ad notice. The actors have 15 days to respond to the notice.

Guardant Health (GH) has seen a significant surge in its stock value, driven by recent FDA approval for its products and growing momentum in the cancer screening market. This development positions the company for potential growth in the healthcare sector.

Maharashtra FDA commissioner Tukaram Mundhe stated that 'nobody will be spared' after notices were issued to actors Shah Rukh Khan and Ajay Devgn concerning their involvement in a Vimal ad, emphasizing that everyone in the chain is responsible.

Radiopharm has scheduled a meeting with the FDA regarding its brain imaging agent, RAD101.

Mumbai's civic chief praised the Food and Drug Administration (FDA) drive conducted under Tukaram Mundhe, stating that society sometimes requires such 'shocks'.

Bollywood actors Shah Rukh Khan, Ajay Devgn, and Tiger Shroff have reportedly received notices from the FDA regarding their involvement in a Vimal Elaichi advertisement.

Shah Rukh Khan and Ajay Devgn defended their association with a controversial brand's advertisements, even as the Maharashtra FDA sent notices to them and Tiger Shroff regarding the Vimal Elaichi ad.

Following reports of cockroaches in Mumbai, a rat was allegedly discovered in a Blinkit ice cream freezer in Thane, intensifying concerns about food safety amidst an FDA crackdown. This incident adds to a series of hygiene issues reported in food establishments.

The FDA has identified jalapeños and eggs as the sources for two of the four active Salmonella outbreaks currently under investigation, leading to product recalls.

The Maharashtra Food and Drug Administration has suspended 14 licenses belonging to quick-commerce platforms Zepto, Blinkit, and Instamart outlets.

FDA officials have finally visited the Taylor Farms facility in Mexico, a month after the site was linked to an outbreak of cyclospora, a parasite causing explosive diarrhea. The visit aims to investigate the source of the contamination.

India's weather body rectified a typing mistake at the Safdarjung observatory, clarifying that Delhi did not exceed its monthly rainfall average in a week, as was temporarily indicated.

Co-Diagnostics has outlined its submission for FDA dual 510(k) and CLIA waiver, as the company's cash reserves have fallen to $3.6 million.

Zoetis shares increased after the FDA granted Emergency Use Authorization (EUA) for its Simparica TRIO drug to treat New World screwworm.

Novartis Pharmaceuticals Corporation has issued a nationwide recall for certain heart failure and high blood pressure medications due to potency issues, as announced by the FDA.

A film industry body has requested the Maharashtra FDA to conduct raids on Mumbai film sets due to concerns over unhygienic, stale, and substandard food being provided to crew members.

The FDA has introduced two structural changes to its Real-World Evidence Guidance, broadening the types of data sponsors can submit, though many in the industry are not yet prepared to utilize these changes.

A former acting commissioner of the FDA and deputy director of the CDC discussed the public awareness timeline of the cyclospora outbreak and broader food safety concerns.

The U.S. Food and Drug Administration (FDA) has proposed changes to regulations that would require food manufacturers to notify the agency before introducing new ingredients or additives.

India's Food and Drug Administration has suspended the license of a Blinkit dark store in Malad West, Mumbai, citing unhygienic conditions, cockroach infestations, and improper food storage on rusted racks and floors.

The Bombay High Court has ordered Amazon to hand over expired goods to the Maharashtra FDA for disposal, following action against Amazon Retail India's warehouse for allegedly distributing expired food.

The FDA is currently evaluating whether six experimental peptides should be made available through compounding pharmacies, with a decision pending on their authorization.

India's Food and Drug Administration (FDA) has seized sub-standard edible oil worth Rs 1.94 crore in Beed and subsequently suspended the licenses of five establishments involved.

Workers in Ogun State are decrying the prolonged closure of distilleries by NAFDAC, appealing to the Federal Government for intervention to alleviate the hardship caused by the ban.

NRx Pharma's stock saw an increase following the FDA's completion of its initial review for the company's ketamine product. This development marks a significant step for the pharmaceutical firm.

Several companies, including Recruit Holdings, Daimler Truck, Arteris, and ICU Medical, have updated or raised their financial outlooks for fiscal year 2026. These revisions reflect various factors such as strong performance, strategic initiatives, and market conditions.

Nigeria's NAFDAC has issued an alert to citizens regarding the circulation of counterfeit Forxiga, a diabetes drug, which poses significant health risks.

The U.S. FDA has granted approval for Moderna's mRNA flu vaccine, marking the first mRNA-based flu shot to receive such clearance. This approval is considered significant for future vaccine development.

The Food and Drug Administration (FDA) in India has revoked the license of the ayurvedic pharmaceutical company Inducare Pharma Pvt Ltd.

OraSure Technologies projects its third-quarter revenue to be between $29.5 million and $32.5 million, while also announcing a delay in the FDA clearance for its InteliQuick CT/NG product beyond 2026.

Merck's application to expand the U.S. label for its RSV shot, Enflonsia, has been accepted by the FDA for review, potentially broadening its use.

GRAIL expects an FDA advisory committee meeting in the fall and is projecting potential approval for its product in the first part of 2027, indicating progress in its regulatory pathway.

The U.S. Food and Drug Administration has given its approval for Moderna's mRNA-based influenza vaccine, marking a significant development in flu prevention.

Nigeria's NAFDAC has advised consumers on four crucial things to check on food labels before purchasing packaged food to ensure healthier choices.

Noor Mohammadi, Shalimar, and K Rustom, popular restaurants in Mumbai, are set to reopen after the FDA stayed their license suspensions.

Biopharmaceutical company Oculis has announced positive feedback from the U.S. Food and Drug Administration (FDA) regarding its plans to develop Privosegtor, a drug substance intended for the treatment of acute multiple sclerosis exacerbations.

Nigeria's National Agency for Food and Drug Administration and Control (NAFDAC) has joined a £3.7 million Oxford-led global vaccine safety project aimed at strengthening vaccine surveillance and boosting public confidence against fake and substandard vaccines.

On 'Last Week Tonight,' John Oliver stated that Taco Bell has the moral high ground over the Trump administration amid a parasite crisis, blaming cuts to the FDA and CDC.

Johnson & Johnson has secured FDA approval for its new surgical robot, Ottava, after years of development and significant investment, aiming to challenge existing competitors in the operating room technology market.

Nigeria's National Agency for Food and Drug Administration and Control (NAFDAC) has reiterated its commitment to banning the sale of sachet alcoholic drinks, citing public health concerns over commercial interests.

Shares of Replimune surged significantly after FDA advisers provided a positive recommendation for the company's skin cancer drug.

An iceberg spotted in Skagafjörður, Iceland, is reportedly melting 20 kilometers out at sea, captured in photographs by Halldór Gunnar Hálfdansson.

Bristol Myers Squibb (BMS) has been granted FDA review for a label expansion of its anemia therapy, developed in partnership with Merck.