Coordination Towards Packaging Development Executive Packaging DevelopmentPacking Executive
Technical Aspects of Packing Coordination (Pharmaceuticals)1. Artwork Management;Management of artwork creation, revision & approval as per regulatory guidelines (EMA, WHO, CDSCO).Checking legibility, font size, barcodes, Braille text (where applicable).Ensuring compliance of carton, foil, label information with approved dossier (MA File).Control on master packing record (MPR) & batch packing record (BPR).2. Packing Material SpecificationsDefining & maintaining specifications for primary, secondary & tertiary packaging:Primary: Blister foil, alu-alu foil, PVC/PVDC, bottles, caps, induction seals etc.Secondary: Cartons, labels, leaflets, shrink wraps etc.Tertiary: Shippers, stretch film, pallets etc.Verification of DMF (Drug Master File)/COA of packing materials.Compatibility check of registered packing with respect to existing formulation machine suitability. 3. GMP & Regulatory CompliancePacking operations to be executed as per cGMP (EU-GMP, MHRA & Schedule M).
Galpha Laboratories is a leading manufacturing and marketing company of pharmaceutical formulations (Finished Dosage Forms) in India.
We express gratitude for our strong foothold in the international market of regulated and emerging healthcare services. The company strives to move forward on a promising path by strategically expanding its business, strengthening its core manufacturing facilities, and enhancing its capabilities. We also look forward to boosting the companys revenue by discovering new markets and close collaborations with our business partners worldwide.
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