QRC Solutions specialises in assisting biotech and life sciences companies to commercialise their technology.
Writing of business documentation including business plans, MOUs, grant applications, etc.
Writing of clinical trial documentation including protocols, investigator's brochures, patient information brochures, etc.
Establishment of quality management systems to a range of national and international standards (e.g. ISO 9001, ISO 13485, etc).
Writing regulatory submissions to seek marketing clearance or approval for a new technology.
Liasing with the relevent regualtory authority.