Ropack Announces Immediate Clinical Trial Distribution Services Capacity For Drug Manufacturers

At Ropack, clinical trial distribution is one of our most –requested services. Many of the most respected pharmas and CROs rely on us to meet their in-Canada clinical study needs, from packaging and expiration date relabeling to distribution, tracking, collection and certified destruction or storage of materials.

To maintain superior quality Ropack has skilled, responsive staff and cGMP-compliant facilities:

• Qualified, responsive staff members working in teams to ensure a cohesive process
• 33,000 sq. ft. within a FDA and Health Canada inspected facility, with 1,500 sq. ft. of office space
• Ample storage, including two 26’ x 70’ SuperSaver receptacles
• Refrigerated rooms with up to 300 pallet locations
• The ability to handle controlled substances and dangerous goods
• Two Level 9 controlled-substance storage vaults
• Five individual and segregated order-fulfilling and verification stations
• Comprehensive cold chain management, 2º degrees C to 8º degrees C

• Flexible and adaptable regulatory process to meet your needs.
• Ropack can meet Canadian and FDA cGMP regulations.
• Consolidated shipments that reduce costs
• Shortened go-to-market timelines.

ROPACK PHARMACEUTICAL CLINICAL DISTRIBUTION DEPOT

• 33 000+ sq. ft. of command and control
• Five individual and segregated shipper assembly lines

Ample Storage:

• Two 70'x26' SuperSaver receptacles
• Two level 9 controlled substance vaults

Comprehensive Cold-Chain Management:

• 190 pallet locations at 2 °C to 8 °C
• Specialized teams for a cohesive process
• Secondary packaging and labeling of supplies.
• Up to 96-hour pre-qualified shipping system