Skip to main content

Pharma News

Get the latest news from world and India’s leading pharmaceutical companies Pharma Industry, pharmaceutical marketing, generic drugs, and Complete news for Pharmacy and Life Sciences professionals.

  • In the meeting, the MoS stressed on the need to increase the Viral Research Diagnostics Laboratories (VRDL) in the states, including UP. Smt. Anupriya Patel, Minister of State (Health & Family Welfare), in a high level meeting, reviewed the activities and achievements of Department of Health Research (DHR) and Indian Council of Medical Research (ICMR).  Dr. Sanjay Mehendale, Additional Director General, ICMR and Smt. Sarita Mittal Joint Secretary, Department of Health Research were also present.

  • The U.S. Food and Drug Administration announced the voluntary destruction and recall of a large volume of kratom-containing dietary supplements manufactured and distributed nationwide under the brand names Botany Bay, Enhance Your Life and Divinity by Divinity Products Distribution of Grain Valley, Missouri. In cooperation with the FDA, the company has also agreed to stop selling all products containing kratom.

  • In the 78th meeting of the Drugs Technical Advisory Board (DTAB) held on 12th February, 2018 under the Chairmanship of the Director General of Health Services deliberated the directions of the Hon’ble Supreme Court of India dated 15.12.2017 in regard to the notifications issued by the Govt, of India prohibiting 344 FDCs +05 FDCs vide S.O.No. 705(E) to 1048 (E) dated 10.03.2016 and S.O. No. 1851(E) to 1855(E) dated 08.06.2017 respectively.

  • The Central Drugs Standard Control Organisation (CDSCO) has decided to make the regulations more stringent to tackle the menace of the widespread misuse of Oxytocin, a neurotransmitter and peptide hormone, in dairy and horticulture industry crop up on a daily basis. The Regulatory body will hold a crucial meeting on February 22 at 11:00Am in Delhi with all the manufacturers of Oxytocin formulation for human and animal use in the country.

  • FDA amended its regulations on the acceptance of data from clinical investigations for medical devices. The rule updates the FDA’s standards for accepting clinical data from clinical investigations conducted both inside and outside the United States to help ensure the protection of human participants, and to help ensure the quality and integrity of data obtained from these clinical investigations.

  • The genetic cause behind a strain of typhoid’s resistance to five classes of antibiotics has been uncovered by scientists at the Wellcome Sanger Institute and their collaborators at Public Health England and Aga Khan University, Pakistan. There is currently a major outbreak of typhoid fever in Pakistan, and there was a case in the UK following air travel, which has been isolated and treated. This study shows the typhoid strain causing the outbreak acquired an additional piece of DNA to become resistant to multiple antibiotics, including a third-generation antibiotic.

Subscribe to Pharma News