Development Gmp Compliant Sterile Production Area Tender Notice
Description
Develop a GMP compliant sterile production area on a turnkey basis including a state of the art clean room facility in accordance with DRAP regulatory requirements for validation and qualification of sterile production operations. The facility shall include two production lines with capacities of 6000 vials per batch and 1000 vials per batch. Bids shall be submitted under the Two Stage-Two Envelope procurement procedure. Qualified EPC contractors registered with FBR are eligible to participate. Tender documents may be obtained during working hours upon payment of the prescribed non-refundable tender fee through CDR or Bank Draft. Bid opening will take place at 11:00 AM. Pro Tip: The project covers clean room construction, GMP compliance, sterile manufacturing facilities, pharmaceutical production, EPC contracting, validation, qualification, process engineering and pharmaceutical infrastructure development.
Organization Contact
Tags
construction, pharma
Keywords Used for Search
development gmp compliant sterile production areaClosing Date: 14 Jul 2026
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