GMP Consulting Supports FDA Audits, SOPs, Testing, and GMP Readiness for Supplement Manufacturers IRVINE, CA, UNITED ...

IRVINE, CA, UNITED STATES, March 17, 2026 /EINPresswire.com/ — Qalitex Laboratories, an ISO 17025-accredited third-party analytical testing laboratory serving pharmaceutical developers, contract ...

SK pharmteco today announced the successful conclusion of a regulatory inspection of its small molecule North America facility in La Porte, Texas.

March 17 (Reuters) - The U.S. Food and Drug Administration declined to approve Aldeyra Therapeutics' drug for a type of eye disease, the company said on Tuesday, sending its shares plunging over 70% ...

FDA replaces seven fragmented adverse event databases with AEMS, enabling real-time safety signal access for pharmaceutical manufacturers and researchers. On March 11, the FDA launched a unified ...

The Jammu and Kashmir High Court has dismissed criminal proceedings initiated against a pharmaceutical company based in ...

Novo Nordisk issued a response to an FDA warning letter that cited serious violations in how the company tracked and reported ...

The Food and Drug Administration (FDA) has supervised the destruction of recalled batches of NAN OPTIPRO and NANKID OPTIPRO ...

DUBAI, 17th March, 2026 (WAM) -- The Emirates Drug Establishment (EDE) has affirmed that the UAE’s strategic stockpile of medicines and medical supplies is secure and sufficient to meet local market ...

The FDA has faced an extraordinary convergence of political, scientific, legal, and operational pressures over the last year.