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The WORLD HEALTH ORGANIZATION (WHO) has issued a Tender notice for the procurement of a Training and Coaching of Regulatory Inspectors for Who Good Manufacturing Practices on Sterile Pharmaceuticals (readvertisement) in the Philippines. This Tender notice was published on 04 Sep 2026 and is scheduled to close on 17 Sep 2026, with an estimated Tender value of Refer Document. Interested bidders can access detailed Tender information, eligibility criteria, and complete bidding documents by referencing TOT Ref No. 148554130, while the tender notice number is WPRO/DAF/SAO/SUP/P/0009526 and Registering on the platform.
Procurement Summary
Country: Philippines
Summary: Training and Coaching of Regulatory Inspectors for Who Good Manufacturing Practices on Sterile Pharmaceuticals (readvertisement)
Deadline: 17 Sep 2026
Posting Date: 04 Sep 2026
Other Information
Notice Type: Tender
TOT Ref.No.: 148554130
Document Ref. No.: WPRO/DAF/SAO/SUP/P/0009526
Competition: ICB
Financier: World Health Organization (WHO)
Purchaser Ownership: Public
Tender Value: Refer Document
Purchaser's Detail
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Login to see detailsTender Details
National regulatory authorities and ministries of health increasingly require inspectors who can assess sterile pharmaceutical products, vaccines, biotechnology products and other biologicals using a risk-based and evidence-led approach. Sterile manufacturing is a high-risk area because weaknesses in contamination control, aseptic processing, environmental monitoring, sterilization, utilities, data integrity, investigations or CAPA may have direct implications for patient safety and product quality.The underlying concept note recommends a staged, competency-based pathway consisting of self-paced online learning, instructor-led interactive core online course with substantial practical work, and three to six months of regular online mentored follow-up during which 5-working-day in-country training and coached mock inspection led by instructors in two targeted countries including Mongolia and Lao PDR. The course should be grounded primarily in WHO GMP main principles, WHO GMP for sterile pharmaceutical products, WHO GMP for biological products, WHO guidance on quality risk management, validation, water for pharmaceutical use, data integrity, inspection reporting, desk assessment, reli...
Publish Date: 04-Sep-2026
UN Orgnization: WORLD HEALTH ORGANIZATION (WHO)
Type of Notice: Request for proposal
Documents
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