Our Services
Please click on one of our services below for further information
- Sterile services
- Aseptic processing
- Radiopharma (14c radiolabeled)
- Potents (inc. cytotoxics)
- Formulation Development
- Biologicals (non-live)
- Non-sterile services
- Bulk supply of specials
- Testing services
- Clinical packaging
- Production expertise
- Project management
- Quality
- Additional services
- Licenses, equipment & capabilities
packaging.pdf
(277kb)
(277kb)
Clinical packaging services
In addition to our development, manufacturing and filling capabilities, we provide a range of packaging services to suit your clinical trial or commercial project requirements, all to cGMP standards. Whether using our packaging services in conjunction with our production services or in isolation, we deliver finished product worldwide, direct to sites. Our team of experts can provide you with the following packaging solutions -
Labelling and packaging
- Labelling and packaging for Phase I, II and III clinical trials to FDA requirements for the following -
- Individual patient kits
- Blinded or un-blinded patient kits
- Randomised patient kits in various formats including crossover, comparator, parallel etc.
- Labelling and packaging for commercial purposes
- Generation of randomisation lists (designed and generated at SCM pharma or designed by client)
- Bulk packaging and labelling of products and components
- Pack-downs (capsule shells, ampoules, vials, bottle tops, stoppers etc)
- Blister packaging services to suit small volume and complex operations for clinical trial and non-clinical trial use
- Device assembly design and combination pack assembly
- Bespoke design of clinical and non-clinical labels including -
- Foreign language labels
- Barcodes
- Branded labels
- Design of clinical patient kits or packaging for commercial packs
- Design of clinical randomisation lists
Distribution services
- Cold chain distribution
- Overseas distribution direct to study sites - worldwide
Additional services
- Technical packaging consultancy which includes reviewing clinical protocol for accuracy
- Regulatory advice
- Technical support service
- Audit of suppliers
- Equipment and process validation
- QP services
