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Capability
01 Clinical Services (5)
Country
01 France (5)
- Service Details
Eurofins CDMO can provide primary packaging services for non-sterile solid forms (capsules & tablets) in HDPE bottles or blister packagings in class C rooms. They provide a large range of bottles from 15 to 600 mL with several options for caps.
- Directory Listing
Pharma Service: Packaging
Sub Category: Overview
Eurofins CDMO can perform customized labeling and secondary packaging at every clinical trial phase for sterile and non-sterile dosage forms (blisters, blister-cards, vials, syringes, bottles).
Sub Category: Secondary Packaging
Sub Category: Label
Eurofins CDMO provides QP services including all the quality and regulatory support for clinical trial supplies. They can also provide GMP certification, documentation review, audits of manufacturing sites, QP agreement, and final batch release.
Eurofins CDMO (Contract Development & Manufacturing Organization) offers GMP storage of 560 m3 at 15-25°C, 146 m3 at 2-8°C, 2.6 m3 at 20°C and 0.5 m3 at -80°C.