We need you, Through clinical preliminaries, individuals like you, have helped us to enhance and create medicines for asthma, tumor, diabetes, coronary illness, crabby gut disorder and numerous different conditions.
30 years’ clinical trial experience
Remainder Sciences are world specialists in running clinical preliminaries, supporting medicinal headways and making them more straightforward for sufferers to take. All new test meds experience thorough testing before they can be endorsed or sold and the clinical preliminaries we run are a piece of this procedure.
We have 30 years’ experience working clinical preliminaries, amid which time we have been engaged with the advancement of prescriptions for some, key medical problems confronting the UK today and have created authority learning in growing once-a-day solutions and breathed in pharmaceuticals.
Ensuring your safety and well-being (We Need You)
Our best in the class clinical unit is situated in Ruddington, simply outside Nottingham, and highlights the most noteworthy quality offices and hardware, guaranteeing your stay is as unwinding and charming as could be expected under the circumstances. (We Need You)
Your security and prosperity is our essential concern and we have very qualified staff, including specialists, medical caretakers, and professionals at our unit 24 hours every day. We are affirmed and directed by the MHRA (Medicines and Healthcare items Regulatory Agency), who support and screen every single clinical preliminary in the UK. The MHRA additionally frequently surveys everything about how we run our preliminaries to guarantee the wellbeing and solace of our volunteers. An autonomous morals board likewise audits every preliminary that we lead before it starts.
A world-leading reputation for developing medicines of the future of We Need You
WeNeedYou coordinates medication definition improvement, GMP sedate item producing and clinical pharmacology administrations and work with a significant number of the main biotech and pharmaceutical organizations around the world.
Built up in 1990, we utilize more than 700 staff and work from best in class producing and clinical offices in the UK and USA. We have finished more than 1,200 Phase 1 preliminaries and can bolster our customers by working under FDA (Food and Drug Administration) or MHRA (Medicines and Healthcare items Regulatory Agency) rules. We offer a full scope of help administrations, from consider set-up directly through to information examination and announcing.