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GMP APPROVAL
Advit Jewels IPO Day 3: Issue subscribed 213x on strong retail, NII demand; GMP hints at 40% listing gainsJaipur's Advit Jewels IPO is witnessing overwhelming investor interest, subscribed over 212 times by day three, with a significant 40% grey...
Advit Jewels IPO Day 2: Issue subscribed over 20x, GMP signals 41% listing gains. Should you bid?Jaipur-based Advit Jewels' IPO is seeing massive investor interest, subscribed over 20 times on day two with a strong grey market premium. ...
Fredun Pharmaceuticals board approves 2:1 bonus issueFredun Pharmaceuticals’ board has recommended a 2:1 bonus issue, granting two new equity shares for every one held. This decision aims to r...
Anupam Rasayan to acquire up to 43 pc stake in Bliss GVS Pharma for around Rs 1,369 crSpecialty chemicals maker Anupam Rasayan India is set to acquire up to 43.3% of Bliss GVS Pharma for an estimated Rs 1,369.51 crore, with a...
Venus Remedies expands Latin America presence with Argentina nod for antibioticVenus Remedies has received approval in Argentina for its antibiotic Ceftriaxone. This marks a significant step in the company's Latin Amer...
Lord’s Mark among few global players to win HIV self-test approval, exports from June 2026Lord's Mark Industries Ltd. has secured Central Licensing Authority approval for its LordsMed HIV 1&2 Self Test, becoming one of nine globa...
Compliance squeeze, global scrutiny redefine India’s $30 billion pharma export playbookAs global markets prioritise quality and regulatory trust, India’s pharma sector is recalibrating beyond its traditional cost advantage.
Venus Remedies gets GMP approval for pre-filled syringe facilityIndian pharmaceutical company Venus Remedies received a significant approval from the Malaysian authorities. The company's Baddi facility, ...
Biocon Biologics gets EMA nod to produce biosimilar Bevacizumab at Bengaluru plantBiocon Biologics received EMA approval to manufacture biosimilar Bevacizumab in Bengaluru, providing additional capacity to address patient...
Covaxin receives GMP certificate from Hungary: Bharat BiotechBharat Biotech intends to submit documentation for emergency use authorisation to several additional countries worldwide, the company said.
Biocon gets EIR from USFDA for manufacturing facility in BengaluruBiocon on Friday said it has received the establishment inspection report (EIR) from US health regulator for the post-approval and good man...
Lupin Pharma gets Good Manufacturing Certificate for its biologic plantBiosimilar Etanercept is used to fight a range of severe auto-immune disorders.
JB Chemicals & Pharma's Gujarat facilities get European nod"JB Chemicals & Pharmaceuticals is pleased to announce receipt of European GMP approval for its formulation facilities at Panoli, Gujarat f...
Biocon plunges 4% as French regulator decides to re-inspect facilityThe re-inspection will be to verify implementation of the proposed corrective and preventive actions, the company said.
ANSM gives GMP nod to Biocon, to re-inspect drug product unitBiocon, with its partner Mylan, will work with the French and European regulatory authorities with regard to the follow- up inspection of t...
- Shilpa Medicare receives EU GMP approval from Germany
Pharma company Shilpa Medicare on Friday said it has received European Union GMP approval from Germany for two of its manufacturing sites f...
- Unichem gets quality certificate from European Directorate
Unichem Laboratories has received from European Directorate the Quality of Medicines and Healthcare certificate for its active substances p...
- Glenmark Pharmaceuticals gets FDA nod for Baddi plant in HP
Glenmark Pharmaceuticals on Monday said it has received the US Food and Drug Administration's approval for its semi solid dosage manufactur...
- GMPs may take toll on drug exports
In what could hit the country’s vaccine exports estimated to be at Rs 1,500 crore, besides maligning the reputation of Indian companies, WH...
- Glenmark gets UK regulatory nod for its plant
Drug maker Glenmark Pharmaceuticals on Wednesday said it has received approval from the UK regulatory agency for its semi-solid (ointments ...