Our experience ranges from clinical trial and marketing authorizations, price and reimbursement, medical technology, and regulatory strategy services to fixed drug combinations.
Through years of quality assurance activities and quality management system development and implementation we gained thorough insight of GCP, GLP and ISO standards. Our experience ranges from independent reviews and audits to GCP, GLP and ISO standards implementation.
Being aware of raising concerns and corresponding regulatory changes, it was decided to integrate Clinical Research & Post-approval Safety, as well as Medical Devices Safety into Altiora Consulting.
Supporting patent protection and intellectual property rights, merges and acquisitions, contracting and solicitation.
Being focused on its human capital Altiora has developed it's training program. Altiora Consulting is dedicated to share the knowledge by working on innovative methods trying to utilise modern technologies and combine them with traditional learning tools.
Helping in concept and product development, study design, protocol and investigators brochure writing, scientific advice.