Skip to main content

Health Ministry Proposes Acknowledgement-Based Import System for Drug Testing Samples

the Ministry of Health and Family Welfare has proposed amendments to the Drugs Rules, 1945 to simplify the import procedure for drugs intended for examination, testing and analysis.
Government Proposes Major Changes to Medical Devices Rules to Speed Up Licensing
The Ministry of Health and Family Welfare has released draft amendments to the Medical Devices Rules, 2017, proposing significant changes to reduce the time required for granting manufacturing licences for medical devices in India.
Government Pharmacist Recruitment - 09 posts in District Health Society
Diploma In Pharmacy from a recognized institute. Registered under State Pharmacy Council. Computer proficiency (MS Office) & Internet.
Advertisement for the post of Pharmacist at ECHS Central Organization
B.Pharmacy or Approved Diploma in Pharmacy from an Institute recognized by the Pharmacy Council of India and registered as Pharmacist. Minimum 03 years experience. The ECHS Central Organization is located at Delhi and functions under the Chief of Staff Committee through AG and DGDC&W in Army HQ.
Apply Online for Quality Manager at PAREXEL - Work from Home opportunity
Bachelors Degree required preferably in life sciences or health-related discipline or equivalent experience.
IQVIA Require Clinical Data Specialist
Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs.
Eli Lilly Launches Tanstrive in India, Expanding Precision Treatment Options for RET-Altered Cancers

Eli Lilly and Company India has announced the launch of Tanstrive (selpercatinib) in India following marketing authorisation from the Central Drugs Standard Control Organisation (CDSCO). The targeted therapy is indicated for patients with locally advanced or metastatic solid tumours driven by rearranged during transfection (RET) gene alterations, offering a new precision medicine option for eligible cancer patients.

USFDA Completes Pre-License Inspection at Dr. Reddy's Bachupally Biologics Facility; Issues Form 483 with Seven Observations

Dr. Reddy's Laboratories Limited has informed the stock exchanges that the United States Food and Drug Administration (USFDA) has completed a Pre-License Inspection (PLI) at the company's biologics manufacturing facility located in Bachupally, Hyderabad.

According to the company's regulatory filing, the inspection was conducted from June 16 to June 25, 2026. At the conclusion of the inspection, the USFDA issued a Form 483 containing seven observations.

CDSCO Announces Permanent Drug Inspector Recruitment - 186 Openings
Bachelors degree in Pharmacy or Pharmaceutical Sciences or Medicine with specialization in Clinical Pharmacology or Microbiology from a recognized University or institute.
Recruitment for Pharmacist and Scientific Assistant under Public Service Commission
Degree / Diploma course in Pharmacy from a recognized University and registered in the State Pharmacy Council.