Cabinet approves the Policy for the Medical Device Sector
Introduction: Policy 2023 intends to support the Medical Device industry’s orderly expansion in order to satisfy the public health goals of access, affordability, quality, and innovation in India. The policy puts forth a plan for the industry’s rapid expansion in […]
Read MoreCosmetic Medicine Are Now Under Stricter Regulation
A guideline to strengthen oversight of the medical cosmetology industry was recently released by eleven central departments, including the State Administration for Market Regulation, the National Health Commission, and the Ministry of Public Security. The regulation are to control the […]
Read MoreFDA Approved for Drug To Treat Alzheimer’s Agitation Symptoms with Dementia
The FDA approved Rexulti (brexpiprazole) oral tablets are supplementary approval for the treatment of agitation associated with dementia caused by Alzheimer’s disease. This is the first therapy option for this indication that has FDA Approved. DementiaDementia is a severe and […]
Read MoreMeasures are Taken To Enhance Healthcare.
China’s most recent policy or regulation initiatives to strengthen its national healthcare service system will facilitate the provision of high-quality healthcare services at the community level, assist in resolving issues that these regulation concern the public most in the sector, […]
Read MoreFDA Approval for OTC Hearing Aids
Hearing loss affects 30 million adults in the US, with a high number of people affected by it. Only one-fifth of those who could benefit from a hearing aid seek intervention. To increase access to hearing aids, the FDA Approval […]
Read MoreFDA Regulations Advance Decentralized Clinical Trials
The FDA Regulations is adopting further measures to facilitate the use of decentralized clinical trials (DCTs), in which part or all trial-related activities take place at places other than conventional clinical trial sites, including medicines, biologics, and devices. The government […]
Read MoreThe EU MDR Extended Transition Period is Acknowledged By The TGA Regulations
This article deals with the TGA regulations will acknowledges the prolonged transition period for the EU Medical Device Regulation. The EU extended the EU MDR transition period (external site for devices moving to the EU MDR) from May 26, 2024, […]
Read MoreEngagement of Consultant Companies for FDA Business
The FDA is aware that a number of businesses or individuals provide services linked to FDA rules, such as helping with product approvals or offering guidance on regulatory compliance. It is important to remember that the FDA has not approved […]
Read MoreFirst Respiratory Syncytial Virus (RSV) Vaccine Approved by FDA
This article deals with the first respiratory syncytial virus (RSV) vaccine approved by the FDA Medical Device Regulation. Arexvy is the first respiratory syncytial virus (RSV) vaccine that the FDA Medical Device Regulation has licensed for use in the country. […]
Read MorePhilippines FDA Regulations Warns Against Purchasing and Using Unnotified Medical Devices
This article deals with the Food and Drug Administration (FDA) regulations warning all healthcare professionals and the general public not to purchase and use unnoticed medical device products such as The FDA regulations confirmed that the above-mentioned medical device product had […]
Read More