About Rapidd™
- Benefits
- Services
API
Analytical
- Method Development & Validation
- API & Drug Product Stability
Drug Product
- Formulation Development
- Product Manufacture, Packaging, Labelling & Release
Pre-Clinical Toxicology
Regulatory

Services

Rapidd™ offers the following integrated services required to go from pre-clinical candidate to phase I regulatory submission. The full range of services are summarised below:

API

Toxicology and GMP API Supply
API Isotope Labelling
Solid State Characterisation

Analytical

Method Development & Validation
API & Drug Product Stability (ICH)

Drug Product

Formulation Development
Drug Product Manufacture, Packaging, Labelling & Release

Pre-Clinical Toxicology / Safety Studies

Toxicology
Safety Pharmacology
Bio-analysis
Metabolism

Regulatory

Clinical Trial Application (inc. IB and IMPD preparation)

USA & Europe

Rapidd™ has been designed to offer a fully integrated service to cater for the development needs of companies looking to progress clinical candidates through to IND.

Our typical client base will be located in

Europe
North America
Japan

Of course our full palette of services is available to pharmaceutical companies in all the major markets.

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