Dublin, Jan. 16, 2026 (GLOBE NEWSWIRE) -- The "GMP Auditing for Quality Assurance Training Course for FDA Regulated Industries (Jan 28th - Jan 29th, 2026)" training has been added to ...

DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course" training has been added to ResearchAndMarkets.com's offering. This ...

Dublin, Nov. 05, 2025 (GLOBE NEWSWIRE) -- The "Data Integrity in GMP and GCP: Compliance with FDA, EMA, and MHRA Requirements (Oct 7, 2025)" training has been added to ResearchAndMarkets.com's ...

Dublin, Sept. 18, 2025 (GLOBE NEWSWIRE) -- The "GMP Auditing for Quality Assurance Training Course for FDA Regulated Industries (Oct 20th - Oct 21st, 2025)" training has been added to ...

DUBLIN--(BUSINESS WIRE)--The "Inspection and Audit Readiness Training for Medical Device Manufacturers" training has been added to ResearchAndMarkets.com's offering. Recent US FDA inspections indicate ...

The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course (Jan 22nd - Jan 23rd, 2026)" training has been added to ...

(MENAFN- GlobeNewsWire - Nasdaq) Market opportunities lie in enhancing risk-based V&V planning, focusing on DQ, IQ, OQ, and PQs to address cGMP deficiencies and regulatory expectations. By aligning ...

(MENAFN- GlobeNewsWire - Nasdaq) A significant market opportunity lies in providing comprehensive training on technical documentation for medical device manufacturing, focusing on DHF, DMR, and DHR.

The "Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions Training Course" training has been added to ResearchAndMarkets.com's offering. The World Compliance ...