Pharmaceutical Clinical Trial Services
Our people, delivering your project on time and on budget results in your success
Whether you require a tailor made service to facilitate the transition of your Investigational Medicinal Product (IMP) from development to clinical trial site, a storage solution for your supplies or packing, storage and distribution of commercial supplies, Biotec can help you.
Our pharmaceutical clinical trial services include:-
- Pharmaceutical quality assurance
- Qualified person (QP) services & consultancy
- Pharmaceutical labelling and assembly
- GMP pharmaceutical storage facilities
- Global logistics and trial management
From a single centre, single country to a multi-centre, multi-country trial we have the flexibility to deliver your project on time and on budget. Our dedicated Project Managers will oversee your trial, liaising with you to ensure everything runs smoothly and your clinic timelines are always met.
Working to both EU and US standards, one of our key features is our ability to respond quickly and effectively to our customers changing needs. We pride ourselves on our reliable, flexible and innovative approach to our clients requests and always aim to exceed client expectations throughout the study.
From Phase I-IV clinical studies through to commercial supply, our core services include:
- QP certification and consultancy services
- Clinical Supplies Project Management
- Bespoke clinical packaging design
- Label design and printing
- Patient kit labelling and assembly
- Comparator sourcing
- Storage over a wide range of temperatures
- Global cold chain logistics and distribution
- Return of supplies, reconciliation, storage and destruction.
- Sample collection, reconciliation, storage and shipment to testing laboratories
Partnering with Biotec pharmaceutical trial services ensures adding value.
- Improving the timescales for route to market
- Facilitating a quick and smooth import into the European Union
- Effective relationships between Biotec and client Project Managers, interpreting protocols and converting to finished supplies
- Optimal patient kit design resulting in cost savings
- Supplies to the patient on time
We can also facilitate the manufacture, primary packaging and associated analytical testing via our approved sub-contractors.
For further information regardign our pharmaceutical clinical trial services, simply contact us
Latest news at Biotec
Registered in Wales No. 3483808
Registered Office: Biotec Services International Limited, Biotec House, Central Park, Western Avenue, Bridgend Industrial Estate, Bridgend CF31 3RT UK
© Copyright 2009 Biotec