AstraCrux Clinical Trial and Consulting is a unique company where law overlaps with clinical science. We have experienced and talented staff who want to assist in advancing medical knowledge and to speed up the delivery of treatments to those in need.
AstraCrux assists pharmaceutical & biotechnology companies and CRO clients by drafting and negotiating clinical trial agreements, as well as finding prompt solutions to other contractual obstacles involved in running clinical projects and conducting research.
We help our clients to identify the potential threats to their assets and to reduce these threats to match the acceptable risk level that suits the company's objectives. When it is understood and quantified, risk can be managed, giving a business an advantage against less well-prepared rivals.
AstraCrux is able to connect our clients with worldwide players in the pharmaceutical industry. We have the expertise to evaluate and propose the most suitable opportunities, be it from the perspective of a buyer or that of a supplier.
Medical science consulting services are offered through our alliance network, with a special focus on the Greater China Region.
With experienced experts in the medical device and pharmaceutical industry, AstraCrux provides integrated regulatory solutions in Taiwan and the ASEAN markets.
Through strategic drug development planning, accelerate the path of new drugs to the market.
Reduce the legal risk of the entire drug development process through pre-assessment and in-process consulting for each key milestone.
By engaging professional consultants in a synergistic way, be the best drug development partner for our clients.