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.

The move comes months after the Trump administration touted leucovorin as a potential therapy for a broader group of patients with autism symptoms.

The FDA is planning to only ask for one pivotal clinical trial instead of the long standard of two trials for drug approval. The present FDA commissioner believes it carries the same statistical power ...

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% ...

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

By Michael Erman and Puyaan Singh March 5 (Reuters) - A senior FDA official called UniQure's experimental treatment for ...

COPENHAGEN, March 10 (Reuters) - Novo Nordisk said on Tuesday it had received a warning letter from the U.S. Food and Drug ...

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.